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Mayo Clinic Laboratories (Mayo Clinic)

General information

Mayo Clinic Laboratories
Mayo Clinic
3050 Superior Drive NW
Rochester
Minnesota
United States - 55901
https://www.mayocliniclabs.com/
Organization ID: 500068

Personnel

View this laboratory in GTR

Assertion criteria

Level: Assertion criteria provided

Summary of submissions to ClinVar

Total submissions: 19392

Gene

GeneSubmissionsLast Updated
AAAS6Nov 11, 2024
AARS115Nov 11, 2024
AARS210Nov 11, 2024
AASS7May 23, 2018
ABAT17Nov 11, 2024
ABCA126Nov 11, 2024
ABCB1128Nov 11, 2024
ABCB428Nov 11, 2024
ABCB615Nov 11, 2024
ABCB79Oct 15, 2018
ABCC232Nov 11, 2024
ABCC45Nov 11, 2024
ABCC61Nov 11, 2024
ABCC81Feb 28, 2018
ABCC96Nov 11, 2024
ABCD120Nov 11, 2024
ABCD22May 23, 2018
ABCD33May 23, 2018
ABCD41Dec 21, 2023
ABCG533Nov 11, 2024
ABCG844Nov 11, 2024
ABHD124Nov 11, 2024
ABHD14A-ACY16Dec 21, 2023
ABHD53Nov 11, 2024
ACACA14Nov 11, 2024
ACAD81Dec 21, 2023
ACAD919Nov 11, 2024
ACADM6Nov 11, 2024
ACADS9Nov 11, 2024
ACADSB1Dec 21, 2023
ACADVL26Nov 11, 2024
ACAT11Nov 11, 2024
ACD3Nov 11, 2024
ACE1Nov 11, 2024
ACO15Nov 11, 2024
ACO211Nov 11, 2024
ACOX113Nov 11, 2024
ACOX21Jul 18, 2018
ACOX312Sep 15, 2023
ACP25May 23, 2018
ACSF34Jan 5, 2024
ACTA25Nov 11, 2024
ACTA2-AS12Nov 11, 2024
ACTC14Nov 11, 2024
ACTN15Nov 11, 2024
ACTN219Nov 11, 2024
ACTN41Dec 21, 2023
ACVRL153Nov 11, 2024
ACY16Dec 21, 2023
ACYP12Jan 5, 2024
ADA6Nov 11, 2024
ADA24Nov 11, 2024
ADAM172Dec 21, 2023
ADAMTS105Nov 11, 2024
ADAMTS1380Nov 11, 2024
ADAMTS1713Nov 11, 2024
ADAMTS244Nov 11, 2024
ADAR2Nov 11, 2024
ADARB11Nov 11, 2024
ADCY11Nov 11, 2024
ADCY104Nov 11, 2024
ADCY67Dec 21, 2023
ADGRG17Nov 11, 2024
ADGRG68Dec 21, 2023
ADGRV114Nov 11, 2024
ADORA11Nov 11, 2024
ADSL8Nov 8, 2024
AEBP123Nov 11, 2024
AFG3L217Nov 11, 2024
AGA10May 26, 2021
AGA-DT3May 23, 2018
AGK4Nov 11, 2024
AGL83Nov 11, 2024
AGO11Feb 28, 2018
AGPAT25Nov 8, 2024
AGPS4May 23, 2018
AGRN21Nov 11, 2024
AGXT6Nov 11, 2024
AHDC11Feb 28, 2018
AHNAK1Feb 28, 2018
AHNAK22Jul 18, 2018
AHSP1Nov 11, 2024
AIFM112Nov 11, 2024
AIRE3Nov 11, 2024
AK12Dec 21, 2023
AK22Nov 11, 2024
AKAP914Dec 21, 2023
AKR1D12Dec 21, 2023
AKT21Dec 21, 2023
ALAD1Dec 21, 2023
ALAS22Dec 21, 2023
ALDH18A18Nov 11, 2024
ALDH3A213Nov 11, 2024
ALDH5A17Nov 11, 2024
ALDH7A16Nov 11, 2024
ALDOA19Nov 11, 2024
ALDOB6Nov 11, 2024
ALG14Nov 11, 2024
ALG111Jan 5, 2024
ALG121Feb 28, 2018
ALG133Dec 21, 2023
ALG23Nov 11, 2024
ALG61Nov 11, 2024
ALG84Dec 21, 2023
ALG91Dec 21, 2023
ALK2Nov 11, 2024
ALPI3Nov 11, 2024
ALPK314Nov 11, 2024
ALPL6Nov 11, 2024
ALS29Nov 11, 2024
AMACR23Nov 11, 2024
AMN1Dec 21, 2023
AMPD18May 23, 2018
AMPD22Nov 11, 2024
AMT2Nov 8, 2024
ANAPC152Dec 21, 2023
ANG1Jan 5, 2024
ANK1129Nov 11, 2024
ANK217Nov 11, 2024
ANK31Feb 28, 2018
ANKRD13Jul 7, 2022
ANKRD112Feb 28, 2018
ANKRD2621Nov 11, 2024
ANKS62Dec 21, 2023
ANKZF12Nov 11, 2024
ANLN1Nov 11, 2024
ANO103Nov 11, 2024
ANO31Nov 11, 2024
ANO523Nov 11, 2024
ANO66Nov 11, 2024
ANXA112Nov 11, 2024
AOPEP6Dec 21, 2023
AP3B113Nov 11, 2024
AP3D124Nov 11, 2024
AP4B14Jul 7, 2022
AP4B1-AS13Jul 7, 2022
AP4E19Nov 11, 2024
AP4M110Dec 21, 2023
AP4S14Jul 7, 2022
AP5Z137Nov 11, 2024
APC229Nov 11, 2024
APOA16Nov 11, 2024
APOA1-AS5Nov 11, 2024
APOA21Nov 8, 2024
APOA54Nov 11, 2024
APOB38Nov 11, 2024
APOC21Nov 11, 2024
APOC4-APOC21Nov 11, 2024
APOE7Nov 11, 2024
APP3Nov 11, 2024
APTX13Nov 11, 2024
ARFGEF214Nov 11, 2024
ARG11Nov 11, 2024
ARHGAP242Nov 11, 2024
ARHGAP351Feb 28, 2018
ARHGEF1023Jan 5, 2024
ARHGEF91Jul 7, 2022
ARPC1B5Nov 11, 2024
ARSA26Nov 11, 2024
ARSB20Nov 11, 2024
ARSH15May 23, 2018
ARSL1Feb 28, 2018
ARX2Dec 21, 2023
ASAH126Nov 11, 2024
ASCC13Nov 11, 2024
ASIC4-AS113Nov 11, 2024
ASL4Nov 11, 2024
ASPM2Feb 28, 2018
ASS11Jun 9, 2022
ASTN29Nov 11, 2024
ASXL31Feb 28, 2018
ATL16Nov 11, 2024
ATL33Nov 11, 2024
ATM89Nov 11, 2024
ATN12Nov 11, 2024
ATP13A247Nov 11, 2024
ATP1A11Nov 11, 2024
ATP1A1-AS11Nov 11, 2024
ATP1A29Nov 11, 2024
ATP1A33Nov 11, 2024
ATP2A110Nov 11, 2024
ATP2C21Feb 28, 2018
ATP5F1A7May 23, 2018
ATP5MC31May 23, 2018
ATP6V0A41Nov 8, 2024
ATP6V1B11Nov 11, 2024
ATP7A20Nov 11, 2024
ATP7B204Nov 11, 2024
ATP8A23Nov 11, 2024
ATP8B18Nov 11, 2024
ATP8B1-AS12Nov 8, 2024
ATPAF24Nov 11, 2024
ATRIP6Nov 11, 2024
ATRIP-TREX16Nov 11, 2024
ATRX2Jul 7, 2022
AUH12Nov 11, 2024
AUTS21Feb 28, 2018
AVP1Nov 11, 2024
AVPR23Nov 11, 2024
AXIN232Nov 11, 2024
B3GALNT21Nov 11, 2024
B3GALT612Nov 11, 2024
B3GAT38Nov 11, 2024
B3GLCT1Feb 28, 2018
B4GALNT113Nov 11, 2024
B4GALT79Nov 11, 2024
B4GAT12Jul 7, 2022
BAAT3Nov 11, 2024
BAG317Nov 11, 2024
BAP12Dec 21, 2023
BARD15Nov 11, 2024
BBS12Nov 8, 2024
BBS103Nov 11, 2024
BCKDHA1Jul 7, 2022
BCKDHB4Nov 8, 2024
BCKDK1Dec 21, 2023
BCL11A3Nov 11, 2024
BCS1L7Dec 21, 2023
BDP15Dec 21, 2023
BHLHE411Nov 11, 2024
BICC12Nov 11, 2024
BICD25Nov 11, 2024
BIN15Nov 11, 2024
BLM4Nov 11, 2024
BLNK2May 26, 2021
BLOC1S33Nov 11, 2024
BLOC1S61Nov 11, 2024
BMP14Nov 11, 2024
BMPR1A17Nov 11, 2024
BMPR26Nov 11, 2024
BOLA34Nov 11, 2024
BPGM1Nov 11, 2024
BRAF8Nov 11, 2024
BRAT12Nov 11, 2024
BRCA1120Nov 8, 2024
BRCA2210Nov 11, 2024
BRIP16Nov 8, 2024
BSCL214Nov 11, 2024
BSND2Nov 11, 2024
BTD1Dec 21, 2023
BTK6Nov 11, 2024
C10orf1051Nov 11, 2024
C10orf553Nov 11, 2024
C11orf6537Nov 11, 2024
C12orf5710Nov 11, 2024
C12orf601Nov 11, 2024
C17orf1072Nov 11, 2024
C1QB1Nov 11, 2024
C1QC1Nov 11, 2024
C1QTNF3-AMACR23Nov 11, 2024
C1R2Nov 11, 2024
C1S1Nov 11, 2024
C22Nov 11, 2024
C2CD31Dec 21, 2023
C359Nov 11, 2024
C51Feb 28, 2018
CA5A10Nov 11, 2024
CABP21Dec 21, 2023
CACNA1A24Nov 11, 2024
CACNA1C16Nov 11, 2024
CACNA1C-AS14Nov 11, 2024
CACNA1D6Nov 11, 2024
CACNA1E3Nov 11, 2024
CACNA1G2Nov 11, 2024
CACNA1H5Nov 11, 2024
CACNA1S25Nov 11, 2024
CACNA2D14Nov 11, 2024
CACNA2D23Dec 21, 2023
CACNB27Nov 11, 2024
CACNB42Jul 18, 2018
CAD7Nov 11, 2024
CADPS1Feb 28, 2018
CALM21Nov 11, 2024
CAMTA11Nov 8, 2024
CAPN13Nov 11, 2024
CAPN317Nov 11, 2024
CARD113Nov 11, 2024
CARD1423Nov 11, 2024
CARMIL21Nov 11, 2024
CARS26Nov 11, 2024
CASP106Nov 11, 2024
CASP82Nov 11, 2024
CASQ12Nov 11, 2024
CASR40Nov 11, 2024
CAT5Nov 11, 2024
CATIP-AS24May 23, 2018
CAV35Jul 7, 2022
CAVIN15Nov 11, 2024
CBL4Nov 11, 2024
CBLIF1Dec 21, 2023
CBS22Nov 11, 2024
CC2D2A21Nov 11, 2024
CCDC302Nov 11, 2024
CCDC393Nov 11, 2024
CCDC405Nov 11, 2024
CCDC501Nov 11, 2024
CCDC652Nov 11, 2024
CCDC88C6Nov 11, 2024
CCDST2Feb 28, 2018
CCM23Nov 11, 2024
CCNF2Nov 11, 2024
CCNH3Nov 11, 2024
CCNO2Nov 11, 2024
CCT54Dec 21, 2023
CD1512Nov 11, 2024
CD191Dec 21, 2023
CD272Nov 11, 2024
CD27-AS12Nov 11, 2024
CD3201Nov 11, 2024
CD40LG1May 26, 2021
CD4625Nov 11, 2024
CD552Nov 11, 2024
CD594Nov 11, 2024
CD703Nov 11, 2024
CD79A1Jul 7, 2022
CD79B1May 26, 2021
CDAN147Nov 11, 2024
CDC14A4Dec 21, 2023
CDCA71Nov 11, 2024
CDCA7L2Nov 8, 2024
CDH143Nov 11, 2024
CDH239Nov 11, 2024
CDHR11Feb 28, 2018
CDIN16Nov 11, 2024
CDK5RAP23Feb 28, 2018
CDKL51Jul 7, 2022
CDKN1B1Dec 21, 2023
CDKN2A1Dec 21, 2023
CEACAM162Dec 21, 2023
CEACAM16-AS12Dec 21, 2023
CEBPE2Nov 11, 2024
CENPT1Jul 7, 2022
CEP1041Nov 11, 2024
CEP1201Nov 11, 2024
CEP1643Nov 11, 2024
CEP2908Nov 11, 2024
CEP632Nov 11, 2024
CEP783Nov 11, 2024
CEP832Nov 11, 2024
CEP85L2Dec 21, 2023
CERS12May 26, 2021
CETP4Nov 11, 2024
CFAP923Nov 11, 2024
CFB14Nov 11, 2024
CFD9Dec 21, 2023
CFH78Nov 11, 2024
CFHR115Nov 11, 2024
CFHR214Nov 11, 2024
CFHR317Nov 11, 2024
CFHR420Nov 11, 2024
CFHR540Nov 11, 2024
CFI42Nov 11, 2024
CFL23Nov 11, 2024
CFTR263Nov 11, 2024
CFTR-AS118Nov 11, 2024
CHAT19Nov 11, 2024
CHCHD104Nov 11, 2024
CHD22Dec 21, 2023
CHD31Feb 28, 2018
CHD78Nov 8, 2024
CHEK227Nov 11, 2024
CHIT116May 23, 2018
CHKB1Feb 28, 2018
CHKB-CPT1B1Feb 28, 2018
CHMP2B2Nov 11, 2024
CHPT13Jul 7, 2022
CHRNA23May 26, 2021
CHRNA410Nov 11, 2024
CHRNB21Dec 21, 2023
CHRND3Nov 11, 2024
CHRNE4Nov 11, 2024
CHRNG1Feb 28, 2018
CHST148Nov 11, 2024
CHST61Feb 28, 2018
CHST82Jul 7, 2022
CHSY11Dec 21, 2023
CIB22Dec 21, 2023
CIDEC3Nov 11, 2024
CIITA1Dec 21, 2023
CLCF16Nov 11, 2024
CLCN120Nov 8, 2024
CLCN41Nov 11, 2024
CLCN51Nov 11, 2024
CLCNKA4Nov 11, 2024
CLCNKB3Nov 11, 2024
CLDN11Nov 11, 2024
CLDN141Dec 21, 2023
CLDN14-AS11Dec 21, 2023
CLDN161Nov 11, 2024
CLN313Nov 8, 2024
CLN520Nov 11, 2024
CLN611Jun 3, 2024
CLN85Dec 21, 2023
CLPB6Nov 11, 2024
CLPP6Dec 21, 2023
CLPX2Nov 11, 2024
CLTCL17Nov 11, 2024
CNTN12Dec 21, 2023
CNTN21Feb 28, 2018
CNTNAP126Nov 11, 2024
CNTNAP213Nov 11, 2024
COA52May 23, 2018
COA62May 23, 2018
COA87Jan 5, 2024
COASY1Nov 8, 2024
COCH1Dec 21, 2023
COG41May 26, 2021
COG51May 26, 2021
COG77Dec 21, 2023
COG83Dec 21, 2023
COL11A15Nov 11, 2024
COL11A23Dec 21, 2023
COL12A159Nov 11, 2024
COL13A15Nov 11, 2024
COL1A144Nov 11, 2024
COL1A227Nov 11, 2024
COL27A11Feb 28, 2018
COL2A13Nov 8, 2024
COL3A142Nov 11, 2024
COL4A116Nov 11, 2024
COL4A23Nov 11, 2024
COL4A2-AS21Nov 11, 2024
COL4A316Nov 11, 2024
COL4A413Nov 11, 2024
COL4A516Nov 11, 2024
COL4A62Nov 11, 2024
COL5A166Nov 11, 2024
COL5A239Nov 11, 2024
COL6A118Nov 11, 2024
COL6A219Nov 11, 2024
COL6A334Nov 11, 2024
COL7A14Nov 11, 2024
COL9A13Dec 21, 2023
COL9A21Feb 28, 2018
COL9A32Dec 21, 2023
COLQ2Feb 28, 2018
COPA2Nov 11, 2024
COQ213Nov 11, 2024
COQ414Nov 11, 2024
COQ613Nov 11, 2024
COQ72Nov 11, 2024
COQ8A27Nov 11, 2024
COQ8B15Nov 11, 2024
COQ95Nov 11, 2024
CORO1A1Dec 21, 2023
COX1022Nov 11, 2024
COX142Nov 11, 2024
COX156Nov 11, 2024
COX206Nov 11, 2024
COX4I22Nov 11, 2024
COX6A13Nov 11, 2024
COX6A21Nov 11, 2024
COX6B11May 23, 2018
COX7B2May 23, 2018
CP8Nov 11, 2024
CPA61Jul 7, 2022
CPLANE12Nov 8, 2024
CPOX9Nov 11, 2024
CPS12Nov 11, 2024
CPT1A1Nov 11, 2024
CPT1C5Nov 11, 2024
CPT227Nov 11, 2024
CR23Dec 21, 2023
CRB211Nov 11, 2024
CREBBP1Nov 11, 2024
CRLF16Nov 11, 2024
CRPPA3Nov 11, 2024
CRPPA-AS11Jan 5, 2024
CRTAP3Dec 21, 2023
CRYAB4Nov 11, 2024
CSF1R7Nov 11, 2024
CSF2RA1Jul 7, 2022
CSF3R16Nov 11, 2024
CSNK2B2Jul 18, 2018
CSPP11Dec 21, 2023
CSRP33Dec 21, 2023
CST32Nov 11, 2024
CSTB3Nov 8, 2024
CTBP11Nov 11, 2024
CTBP1-AS1Nov 11, 2024
CTC114Nov 11, 2024
CTCF1Jul 18, 2018
CTDP131Nov 11, 2024
CTLA43Nov 8, 2024
CTNNA12Nov 11, 2024
CTNNB11Jul 18, 2018
CTNS13Nov 11, 2024
CTNS-AS17Nov 11, 2024
CTRC26Nov 11, 2024
CTSA18Dec 21, 2023
CTSD14Nov 11, 2024
CTSF15Jan 5, 2024
CTSK2Nov 8, 2024
CUBN26Nov 11, 2024
CWF19L12Nov 11, 2024
CXCR23Nov 11, 2024
CXCR46Nov 11, 2024
CYB561D22Dec 21, 2023
CYB5R37Nov 11, 2024
CYBB2Dec 21, 2023
CYC15May 23, 2018
CYLD-AS11May 26, 2021
CYP21A24Nov 11, 2024
CYP24A13Nov 11, 2024
CYP27A129Nov 11, 2024
CYP2R12Dec 21, 2023
CYP2U110Nov 11, 2024
CYP2U1-AS14Nov 11, 2024
CYP7A14Nov 11, 2024
CYP7B115Nov 11, 2024
D2HGDH18Nov 11, 2024
DAG13Nov 11, 2024
DARS11Nov 11, 2024
DARS236Nov 11, 2024
DBNL8Nov 11, 2024
DCAF171Nov 11, 2024
DCDC23Nov 11, 2024
DCLRE1C5Nov 11, 2024
DCTN116Nov 11, 2024
DCX3Nov 11, 2024
DDHD116Nov 11, 2024
DDHD27Dec 21, 2023
DDX3X3Nov 11, 2024
DDX591Nov 11, 2024
DEF61Nov 11, 2024
DELE11Nov 11, 2024
DEPDC512Nov 11, 2024
DES11Nov 11, 2024
DGAT12Nov 11, 2024
DGAT23Nov 11, 2024
DGKE15Nov 11, 2024
DGUOK13Nov 11, 2024
DGUOK-AS11Jan 5, 2024
DHCR75Nov 11, 2024
DHDDS1May 26, 2021
DHFR2Nov 11, 2024
DHH6Dec 21, 2023
DHTKD117Jan 5, 2024
DIAPH19Nov 11, 2024
DIAPH31Nov 11, 2024
DICER13Nov 11, 2024
DIS3L22Nov 11, 2024
DKC14Nov 11, 2024
DLAT12May 23, 2018
DLD16Nov 11, 2024
DLG41Nov 11, 2024
DMAC2L4Nov 11, 2024
DMD24Nov 11, 2024
DMP13Nov 11, 2024
DMXL22Dec 21, 2023
DNA215Nov 11, 2024
DNAAF15Nov 11, 2024
DNAAF193Dec 21, 2023
DNAAF22Nov 11, 2024
DNAAF32Dec 21, 2023
DNAAF3-AS12Dec 21, 2023
DNAAF41Nov 11, 2024
DNAAF4-CCPG11Nov 11, 2024
DNAAF55Nov 11, 2024
DNAAF61Jul 18, 2018
DNAH116Nov 11, 2024
DNAH1117Nov 11, 2024
DNAH522Nov 11, 2024
DNAH813Nov 11, 2024
DNAH8-AS12Nov 11, 2024
DNAH96Nov 11, 2024
DNAI13Nov 11, 2024
DNAI21Jul 16, 2018
DNAJB111Dec 21, 2023
DNAJB132Nov 11, 2024
DNAJB28Nov 11, 2024
DNAJB63Nov 11, 2024
DNAJC123Dec 21, 2023
DNAJC133Nov 11, 2024
DNAJC193Nov 11, 2024
DNAJC215Nov 11, 2024
DNAJC33Nov 11, 2024
DNAJC55May 23, 2018
DNAJC62Nov 8, 2024
DNAJC9-AS12May 23, 2018
DNAL11Nov 11, 2024
DNASE18Nov 11, 2024
DNASE21Nov 11, 2024
DNM1L10Nov 11, 2024
DNM216Nov 11, 2024
DNMT110Nov 11, 2024
DNMT3B1Nov 11, 2024
DOCK31Feb 28, 2018
DOCK713Nov 11, 2024
DOCK819Nov 11, 2024
DOK715Nov 11, 2024
DOLK2Nov 11, 2024
DPAGT14Dec 21, 2023
DPM14Nov 11, 2024
DRC12Nov 11, 2024
DSC211Nov 11, 2024
DSCAS1Dec 21, 2023
DSE9Nov 11, 2024
DSG216Nov 11, 2024
DSG2-AS18Nov 11, 2024
DSP39Nov 11, 2024
DSP-AS11Nov 11, 2024
DSPP1Nov 11, 2024
DST88Nov 11, 2024
DST-AS11Nov 11, 2024
DTNA4Dec 21, 2023
DTNBP13Nov 11, 2024
DUOX24Nov 11, 2024
DUOXA21Feb 28, 2018
DYNC1H115Nov 11, 2024
DYNC2H13Nov 11, 2024
DYNC2LI126Nov 11, 2024
DYRK1A1Jul 7, 2022
DYSF57Nov 11, 2024
DZIP1L4Nov 11, 2024
EARS214Nov 11, 2024
EBF31Feb 28, 2018
ECH17May 23, 2018
EDN31Nov 11, 2024
EDNRB1Feb 28, 2018
EDNRB-AS11Feb 28, 2018
EEF1A23Jul 7, 2022
EFCAB13-DT1Nov 11, 2024
EFEMP23Nov 11, 2024
EFL13Nov 11, 2024
EGF1Nov 11, 2024
EGFR2Nov 11, 2024
EGILA1Jan 5, 2024
EGLN22Nov 11, 2024
EGR29Nov 11, 2024
EHHADH6Nov 11, 2024
EHMT11Dec 21, 2023
EIF2B11Nov 11, 2024
EIF2B33Nov 11, 2024
EIF2B53Nov 11, 2024
EIF4G14Nov 11, 2024
ELAC220Nov 11, 2024
ELANE12Nov 11, 2024
ELN1Feb 28, 2018
ELP123Nov 11, 2024
EMD1Nov 11, 2024
ENG79Nov 11, 2024
ENO314Nov 11, 2024
ENPP13Nov 8, 2024
ENTPD11Feb 28, 2018
ENTPD1-AS11Feb 28, 2018
ENTPD512Nov 11, 2024
EPAS12Nov 11, 2024
EPB4124Nov 11, 2024
EPB4237Nov 11, 2024
EPCAM1Nov 11, 2024
EPHB11May 26, 2021
EPHB46Nov 11, 2024
EPM2A17Nov 11, 2024
EPM2A-DT8Dec 21, 2023
EPO2Nov 11, 2024
EPOR4Nov 11, 2024
EPS8L22Dec 21, 2023
ERBB39Dec 21, 2023
ERBIN1Nov 11, 2024
ERCC620Jan 5, 2024
ERCC813Nov 11, 2024
ERLIN24Nov 8, 2024
ESPN2Nov 11, 2024
ESR12Nov 11, 2024
ETFA3Nov 11, 2024
ETFB9Nov 11, 2024
ETFDH17Nov 11, 2024
ETHE15May 23, 2018
EVC1Feb 28, 2018
EXT23Nov 11, 2024
EYA42Nov 11, 2024
F105Nov 11, 2024
F1123Nov 11, 2024
F11-AS15Nov 11, 2024
F123Nov 11, 2024
F13A116Nov 11, 2024
F13B4Nov 11, 2024
F24Nov 11, 2024
F54Nov 11, 2024
F739Nov 11, 2024
F868Nov 11, 2024
F917Nov 8, 2024
FA2H13Nov 8, 2024
FADD2Nov 11, 2024
FAH14Nov 11, 2024
FAM111B1Dec 21, 2023
FANCA51Nov 11, 2024
FANCC9Dec 21, 2023
FANCG5Dec 21, 2023
FANCI7Nov 11, 2024
FARS210Nov 8, 2024
FAS6Nov 11, 2024
FASTKD210Nov 11, 2024
FAT18Nov 11, 2024
FBLN55Nov 11, 2024
FBN179Nov 11, 2024
FBN221Nov 11, 2024
FBP16Nov 11, 2024
FBXL39Nov 8, 2024
FBXL419Nov 11, 2024
FBXO111Oct 31, 2017
FBXO386Nov 11, 2024
FBXO412Feb 28, 2018
FBXO74Nov 11, 2024
FBXW71Feb 28, 2018
FCSK1Dec 21, 2023
FDX22Nov 11, 2024
FDX2-ZGLP12Nov 11, 2024
FDXR2Nov 11, 2024
FECH20Nov 11, 2024
FERMT32Nov 11, 2024
FGA16Nov 11, 2024
FGB7Nov 8, 2024
FGD12Jul 7, 2022
FGD411Nov 11, 2024
FGF143Nov 11, 2024
FGF31Dec 21, 2023
FGFR21Nov 11, 2024
FGFR33Jul 7, 2022
FGG16Nov 11, 2024
FH13Nov 11, 2024
FIG426Nov 11, 2024
FKBP101Nov 11, 2024
FKBP148Nov 11, 2024
FKBP14-AS18Nov 11, 2024
FKRP20Nov 11, 2024
FKTN20Nov 11, 2024
FLAD15Nov 11, 2024
FLCN42Nov 11, 2024
FLG2Feb 28, 2018
FLI12Nov 11, 2024
FLNA60Nov 11, 2024
FLNC40Nov 11, 2024
FLNC-AS19Nov 11, 2024
FLT31Oct 17, 2022
FLVCR113Nov 11, 2024
FMO31Dec 21, 2023
FN14Nov 11, 2024
FOLR12Dec 21, 2023
FOXC12Dec 21, 2023
FOXC21Feb 28, 2018
FOXG11Jul 7, 2022
FOXI12Nov 11, 2024
FOXJ12Nov 11, 2024
FOXP33Nov 8, 2024
FOXRED18Nov 11, 2024
FPGT-TNNI3K6Nov 11, 2024
FRAS16Nov 11, 2024
FREM11Nov 11, 2024
FREM22Nov 11, 2024
FRRS1L1Dec 21, 2023
FTCD1Dec 21, 2023
FUCA19Dec 21, 2023
FUS4Nov 11, 2024
FXN4Nov 11, 2024
FYB15Nov 11, 2024
G6PC113May 31, 2024
G6PC37Jan 5, 2024
G6PD22Nov 11, 2024
GAA102Nov 11, 2024
GABRA11Nov 11, 2024
GABRB31Feb 28, 2018
GABRD1May 26, 2021
GABRG22Dec 21, 2023
GALC55Nov 11, 2024
GALE4Nov 11, 2024
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MAPT4Nov 11, 2024
MARK21Feb 28, 2018
MARS115Nov 11, 2024
MARS24Nov 11, 2024
MARVELD21Dec 21, 2023
MASP12Feb 28, 2018
MASP21Feb 28, 2018
MASTL4Nov 11, 2024
MATR32Jul 7, 2022
MBD59Apr 22, 2024
MC1R6Nov 11, 2024
MCCC11Dec 21, 2023
MCM21Dec 21, 2023
MCM3AP15Nov 11, 2024
MCM3AP-AS16Nov 11, 2024
MCM71May 26, 2021
MCOLN111Jul 7, 2022
MCPH11Feb 28, 2018
MECOM1Nov 11, 2024
MECP217Nov 8, 2024
MECR3Nov 11, 2024
MED123Nov 11, 2024
MED12L1Nov 11, 2024
MED171Nov 11, 2024
MED232Nov 11, 2024
MED256Jul 7, 2022
MEFV24Nov 11, 2024
MEGF107Nov 11, 2024
MEN15Nov 11, 2024
MET3Nov 11, 2024
MFAP53Nov 11, 2024
MFF1Nov 11, 2024
MFF-DT16Nov 11, 2024
MFN216Nov 11, 2024
MFSD88Dec 21, 2023
MGAT21May 26, 2021
MGME14Nov 11, 2024
MHRT11Nov 11, 2024
MICU13Nov 11, 2024
MIF4GD-DT3May 26, 2021
MILR17Nov 11, 2024
MIR3936HG2Nov 8, 2024
MIR4733HG1Nov 8, 2024
MIR68861Nov 8, 2024
MITF2Dec 21, 2023
MKKS2Dec 21, 2023
MKS110Nov 11, 2024
MLC13Nov 11, 2024
MLH1132Nov 11, 2024
MLH335Nov 11, 2024
MMAB2Nov 8, 2024
MMACHC25Nov 11, 2024
MME7Nov 11, 2024
MMUT2Dec 21, 2023
MOCS15Nov 11, 2024
MOCS22Dec 21, 2023
MORC23Nov 11, 2024
MPC13May 23, 2018
MPIG6B8Nov 11, 2024
MPL2Nov 11, 2024
MPO2Jul 7, 2022
MPV178Nov 11, 2024
MPZ18Nov 11, 2024
MPZL21Dec 21, 2023
MRAS1Dec 21, 2023
MRE111Dec 21, 2023
MRPL33May 23, 2018
MRPL444Nov 11, 2024
MRPS162May 23, 2018
MRPS222May 23, 2018
MRPS251Nov 11, 2024
MS4A11Nov 11, 2024
MSC-AS11May 26, 2021
MSH2119Nov 11, 2024
MSH39Nov 11, 2024
MSH6176Nov 11, 2024
MSRB31Nov 11, 2024
MSTO15Nov 11, 2024
MTFMT14Nov 8, 2024
MTHFR1Nov 11, 2024
MTM11May 23, 2022
MTMR29Nov 11, 2024
MTO118Nov 11, 2024
MTOR1Dec 21, 2023
MTPAP4May 23, 2018
MTR1Nov 11, 2024
MTRFR8Jan 5, 2024
MTTP15Nov 11, 2024
MUSK5Nov 11, 2024
MUTYH20Nov 11, 2024
MVK14Nov 11, 2024
MVP-DT3May 30, 2024
MYBPC11Nov 11, 2024
MYBPC364Nov 11, 2024
MYH1120Nov 11, 2024
MYH1422Nov 11, 2024
MYH210Nov 11, 2024
MYH610Dec 21, 2023
MYH749Nov 11, 2024
MYH917Nov 11, 2024
MYHAS10Nov 11, 2024
MYL26Nov 11, 2024
MYL35Nov 11, 2024
MYLK20Nov 11, 2024
MYLK-AS13Nov 11, 2024
MYLK22Dec 21, 2023
MYLK34Nov 11, 2024
MYMK1Nov 8, 2024
MYO15A8Dec 21, 2023
MYO18B16Dec 21, 2023
MYO18B-AS13May 26, 2021
MYO192Nov 11, 2024
MYO1E2Nov 11, 2024
MYO3A2Nov 11, 2024
MYO5B3Nov 11, 2024
MYO64Nov 11, 2024
MYO7A5Jan 5, 2024
MYOT5Dec 21, 2023
MYOZ23Jul 7, 2022
MYPN24Nov 11, 2024
NAF14Nov 11, 2024
NAGA16May 30, 2024
NAGLU20Nov 11, 2024
NALCN3Nov 11, 2024
NALCN-AS11Nov 11, 2024
NARS22Nov 11, 2024
NBAS5Nov 11, 2024
NBEA6Nov 11, 2024
NBEAL214Nov 11, 2024
NBN7Nov 11, 2024
NCAPH215Nov 11, 2024
NCF24Nov 11, 2024
NCF44Nov 11, 2024
NCF4-AS11Sep 15, 2023
NDE18Nov 11, 2024
NDRG115Nov 11, 2024
NDST12Feb 28, 2018
NDUFA11May 23, 2018
NDUFA108Nov 11, 2024
NDUFA111Nov 11, 2024
NDUFA121May 23, 2018
NDUFA131Nov 11, 2024
NDUFA22Dec 21, 2023
NDUFA95Nov 11, 2024
NDUFAF111Nov 11, 2024
NDUFAF23Nov 8, 2024
NDUFAF44May 23, 2018
NDUFAF56May 23, 2018
NDUFAF610Nov 11, 2024
NDUFB31May 23, 2018
NDUFB93May 23, 2018
NDUFS117Nov 11, 2024
NDUFS26Nov 11, 2024
NDUFS31May 23, 2018
NDUFS44May 23, 2018
NDUFS61May 23, 2018
NDUFS75May 23, 2018
NDUFS82Dec 21, 2023
NDUFV19Nov 11, 2024
NDUFV22May 23, 2018
NEB64Nov 11, 2024
NECAP11May 26, 2021
NEFH11Nov 11, 2024
NEFL4Dec 21, 2023
NEK12Nov 11, 2024
NEK81Nov 11, 2024
NEU19Nov 11, 2024
NEXMIF1Dec 21, 2023
NEXN10Nov 11, 2024
NF161Nov 11, 2024
NF23Nov 8, 2024
NFKB11Nov 11, 2024
NFU14May 23, 2018
NGF2Jan 5, 2024
NGF-AS12Jan 5, 2024
NGLY13Nov 11, 2024
NHEJ11Jul 7, 2022
NHLRC110Nov 11, 2024
NHP22Jan 5, 2024
NIPA17Nov 11, 2024
NIPSNAP3B4Nov 11, 2024
NKX2-51Feb 28, 2018
NKX6-21Nov 11, 2024
NLRC46Nov 11, 2024
NLRP12Nov 11, 2024
NLRP1217Nov 11, 2024
NLRP315Nov 11, 2024
NOD217Nov 11, 2024
NOTCH130Nov 11, 2024
NOTCH215Nov 11, 2024
NOTCH378Nov 11, 2024
NPC153Nov 11, 2024
NPC23Jan 5, 2024
NPHP16Nov 11, 2024
NPHP312Nov 11, 2024
NPHP3-ACAD1114Nov 11, 2024
NPHP3-AS12Nov 11, 2024
NPHP429Nov 11, 2024
NPHS12Dec 21, 2023
NPHS21Nov 8, 2024
NPRL21Dec 21, 2023
NPRL35Nov 11, 2024
NR1H31May 23, 2018
NR1H46Nov 11, 2024
NR2F13Nov 11, 2024
NR2F1-AS11Feb 28, 2018
NR2F21Feb 28, 2018
NRL18Nov 11, 2024
NRROS3Nov 11, 2024
NRXN110Nov 11, 2024
NSD21Feb 28, 2018
NSUN64Nov 11, 2024
NT5C3A9Jan 5, 2024
NTHL14Nov 11, 2024
NTRK116Nov 11, 2024
NUBPL9Nov 11, 2024
NUP1332Nov 11, 2024
NUP1602Nov 11, 2024
NUP2052Nov 11, 2024
NUP851Dec 21, 2023
OAS11Nov 11, 2024
OAT2Dec 21, 2023
OCLN3Jul 7, 2022
OCRL1Nov 11, 2024
ODAD21Nov 11, 2024
OFD15Nov 11, 2024
OGDH13Nov 11, 2024
OPA135Nov 11, 2024
OPA1-AS12Nov 11, 2024
OPA34Nov 11, 2024
OPTN9Nov 11, 2024
OR10Z15Nov 11, 2024
ORAI15Nov 11, 2024
ORC11Feb 28, 2018
OTC1Dec 21, 2023
OTOA2Dec 21, 2023
OTOF3Dec 21, 2023
OTOG8Dec 21, 2023
OTOGL2Nov 11, 2024
OXCT16Nov 11, 2024
OXCT1-AS11May 23, 2018
OXTR2Jul 7, 2022
P2RY121Nov 11, 2024
P3H11Nov 11, 2024
P3H21Feb 28, 2018
P4HTM1Dec 21, 2023
PACS22Nov 11, 2024
PAFAH1B12Dec 21, 2023
PAH36Nov 8, 2024
PAK32Dec 21, 2023
PALB211Nov 11, 2024
PANK225Nov 11, 2024
PARK71Nov 11, 2024
PARN2Nov 11, 2024
PARS22Nov 11, 2024
PAX11Nov 11, 2024
PAX21Nov 11, 2024
PAX71Dec 21, 2023
PC8Nov 11, 2024
PCCA2Nov 11, 2024
PCCB6Nov 11, 2024
PCDH123Nov 11, 2024
PCDH1510Nov 11, 2024
PCDH191Nov 8, 2024
PCK218Nov 11, 2024
PCNA1Nov 11, 2024
PCSK910Nov 11, 2024
PDCD102Nov 11, 2024
PDE3B2Dec 21, 2023
PDE6D1Dec 21, 2023
PDE8B1Nov 11, 2024
PDGFRA2Nov 11, 2024
PDGFRB3Nov 11, 2024
PDHA12May 23, 2018
PDHB5May 23, 2018
PDHX21Nov 11, 2024
PDK31May 26, 2021
PDP11May 23, 2018
PDSS17Nov 11, 2024
PDSS212Nov 11, 2024
PDYN4Nov 11, 2024
PDYN-AS14Nov 11, 2024
PDZD72Nov 11, 2024
PDZD97Nov 11, 2024
PEPD11Nov 11, 2024
PEX132Nov 11, 2024
PEX1017Nov 11, 2024
PEX11B1May 23, 2018
PEX123May 26, 2021
PEX1311Nov 11, 2024
PEX1413Nov 11, 2024
PEX167Dec 21, 2023
PEX193Nov 11, 2024
PEX24Dec 21, 2023
PEX2611Nov 11, 2024
PEX36Dec 21, 2023
PEX513Nov 11, 2024
PEX627Nov 11, 2024
PEX716Nov 11, 2024
PFKM33Nov 11, 2024
PGAM28Nov 11, 2024
PGAP11Nov 11, 2024
PGAP31Feb 28, 2018
PGBD32Jan 5, 2024
PGK110Nov 11, 2024
PGLS4Nov 11, 2024
PGLS-DT1Nov 11, 2024
PGM124Nov 11, 2024
PHEX1Nov 11, 2024
PHGDH6Nov 11, 2024
PHKA116Nov 11, 2024
PHKA1-AS12Nov 11, 2024
PHKA214Nov 11, 2024
PHKA2-AS11Nov 11, 2024
PHKB34Nov 11, 2024
PHKG25Nov 11, 2024
PHLPP12Feb 28, 2018
PHYH20Nov 11, 2024
PI4KA3Nov 11, 2024
PIEZO1201Nov 11, 2024
PIEZO23Feb 28, 2018
PIGA3Dec 21, 2023
PIGG2Dec 21, 2023
PIGK1Nov 11, 2024
PIGL1Nov 11, 2024
PIGM2Nov 11, 2024
PIGN2Dec 21, 2023
PIGO4Nov 8, 2024
PIGQ1Dec 21, 2023
PIGS2Dec 21, 2023
PIGT3Dec 21, 2023
PIGU1Dec 21, 2023
PIGV5Dec 21, 2023
PIGW2Nov 11, 2024
PIH1D22May 23, 2018
PIK3CD6Nov 11, 2024
PIK3R14Nov 11, 2024
PINK110Nov 11, 2024
PINK1-AS9Nov 11, 2024
PITPNM31Feb 28, 2018
PJVK2Dec 21, 2023
PKD170Nov 11, 2024
PKD1-AS13Nov 11, 2024
PKD212Nov 11, 2024
PKD2L2-DT5Dec 21, 2023
PKHD166Nov 11, 2024
PKLR40Nov 11, 2024
PKP218Nov 11, 2024
PLA2G4A4Nov 11, 2024
PLA2G631Nov 11, 2024
PLAT1Nov 11, 2024
PLAU3Nov 11, 2024
PLCB15Nov 11, 2024
PLCE14Nov 11, 2024
PLCG223Nov 11, 2024
PLCH21May 23, 2018
PLD33Nov 11, 2024
PLEC68Nov 11, 2024
PLEKHG35Nov 11, 2024
PLEKHG531Nov 11, 2024
PLG31Nov 11, 2024
PLN2Dec 21, 2023
PLOD125Nov 11, 2024
PLOD21Nov 11, 2024
PLP14Nov 11, 2024
PLS31Nov 11, 2024
PMM29Nov 11, 2024
PMP21Dec 21, 2023
PMP228Nov 11, 2024
PMPCA2Dec 21, 2023
PMS259Nov 11, 2024
PNKD4May 23, 2018
PNKP24Nov 11, 2024
PNP2Nov 11, 2024
PNPLA29Nov 11, 2024
PNPLA618Nov 11, 2024
PNPLA85Nov 11, 2024
PNPO2Jul 7, 2022
PNPT113Nov 11, 2024
PODXL1Nov 11, 2024
POGLUT11Nov 11, 2024
POLA13Nov 11, 2024
POLD16Nov 11, 2024
POLE20Nov 11, 2024
POLG127Nov 11, 2024
POLG27Nov 11, 2024
POLGARF124Nov 11, 2024
POLR1C9May 23, 2018
POLR2F6Nov 11, 2024
POLR3A7Nov 11, 2024
POLR3B1Nov 11, 2024
POLR3H2Jul 18, 2018
POMGNT113Nov 11, 2024
POMGNT25Dec 21, 2023
POMK3Nov 11, 2024
POMT112Nov 11, 2024
POMT28Nov 11, 2024
POPDC15Dec 21, 2023
PPA22Nov 8, 2024
PPCS2Nov 11, 2024
PPOX12Nov 11, 2024
PPT115Nov 8, 2024
PRADX1May 23, 2018
PRDM127Nov 11, 2024
PRDM164Nov 11, 2024
PRDM56Nov 11, 2024
PREPL2Nov 11, 2024
PRF116Nov 11, 2024
PRICKLE15Jul 7, 2022
PRKACG2Nov 11, 2024
PRKAG217Nov 11, 2024
PRKAR1A1Nov 8, 2024
PRKAR1B3Nov 11, 2024
PRKCD4Nov 11, 2024
PRKCG1Dec 21, 2023
PRKCSH1Dec 21, 2023
PRKG13Dec 21, 2023
PRKN11Nov 11, 2024
PRNP5Nov 11, 2024
PROC44Nov 11, 2024
PRODH2Feb 28, 2018
PROS137Nov 11, 2024
PRRT23May 30, 2024
PRSS110Nov 11, 2024
PRUNE12Nov 11, 2024
PRUNE22Feb 28, 2018
PRX36Nov 11, 2024
PSAP18Nov 11, 2024
PSEN13Nov 8, 2024
PSEN26Nov 11, 2024
PSMB101Nov 11, 2024
PSMB42Nov 11, 2024
PSMB83Jan 5, 2024
PSMG23Nov 11, 2024
PSTPIP13Dec 21, 2023
PTCH14Nov 11, 2024
PTCHD1-AS1Nov 11, 2024
PTEN52Nov 11, 2024
PTGS11Nov 11, 2024
PTPN1124May 30, 2024
PTPRC1Dec 21, 2023
PTPRO2Nov 11, 2024
PTRH21Dec 21, 2023
PTRHD12Nov 11, 2024
PTX31Feb 28, 2018
PUM11Nov 11, 2024
PUS16Nov 11, 2024
PYGL28Nov 11, 2024
PYGM39Nov 11, 2024
PYROXD12Nov 11, 2024
QARS117Nov 11, 2024
RAB181Dec 21, 2023
RAB27A2Nov 11, 2024
RAB33A12Nov 11, 2024
RAB3GAP15Nov 11, 2024
RAB4B-EGLN22Nov 11, 2024
RAB9B4Nov 11, 2024
RAD51B1Dec 21, 2023
RAD51C2Nov 11, 2024
RAD51D3Nov 11, 2024
RAD51L3-RFFL3Nov 11, 2024
RAF110Nov 11, 2024
RAG18Nov 8, 2024
RAG23Dec 21, 2023
RALGAPA16Nov 11, 2024
RANBP23Nov 11, 2024
RAPSN4Nov 11, 2024
RARS14Nov 11, 2024
RARS211Nov 11, 2024
RASA14Nov 11, 2024
RASGRP11Nov 11, 2024
RASGRP21Nov 11, 2024
RB11Nov 8, 2024
RBCK19Nov 11, 2024
RBM2021Nov 11, 2024
RBM8A2Nov 8, 2024
RCCD1-AS11Nov 11, 2024
RECQL45Nov 11, 2024
REEP13Nov 8, 2024
RELN16Jan 5, 2024
RET43Nov 11, 2024
RETREG15Jan 5, 2024
RETREG1-AS11Jan 5, 2024
RFT11Feb 28, 2018
RFXANK1Dec 21, 2023
RHAG12Nov 11, 2024
RIC33Nov 11, 2024
RIF111Nov 11, 2024
RINT12Feb 28, 2018
RIT12Nov 8, 2024
RMND18Nov 11, 2024
RMRP2May 26, 2021
RNASE41Jan 5, 2024
RNASEH13Nov 11, 2024
RNASEH2A1Nov 11, 2024
RNASEH2B2Nov 11, 2024
RNASEH2C2Nov 11, 2024
RNF142Nov 11, 2024
RNF21318Nov 11, 2024
RNF213-AS110Nov 11, 2024
RNF2162Nov 11, 2024
RNF313Nov 11, 2024
RNF431Nov 11, 2024
RNU7-17Nov 11, 2024
ROBO21Nov 11, 2024
ROGDI5Nov 11, 2024
ROR21Feb 28, 2018
RPA11Nov 11, 2024
RPGRIP1L6Nov 11, 2024
RPL36A-HNRNPH215Nov 11, 2024
RPS196Dec 21, 2023
RPS6KA31Feb 28, 2018
RRM2B11Nov 11, 2024
RS11Jul 7, 2022
RSPH12Nov 8, 2024
RSPH31Nov 11, 2024
RSPH4A6Nov 11, 2024
RTEL145Nov 11, 2024
RTEL1-TNFRSF6B45Nov 11, 2024
RTN28Nov 11, 2024
RTN4IP11Nov 11, 2024
RUBCN8Nov 11, 2024
RUNX11Nov 8, 2024
RUNX1-AS11Nov 8, 2024
RUVBL11Nov 11, 2024
RXYLT12Nov 11, 2024
RYR170Nov 11, 2024
RYR243Nov 11, 2024
RYR33Feb 28, 2018
SACS120Nov 11, 2024
SAMD9L6Nov 11, 2024
SAMHD11Nov 11, 2024
SARS216Nov 11, 2024
SBDS7Nov 11, 2024
SBF154Nov 11, 2024
SBF226Nov 11, 2024
SBF2-AS13Nov 11, 2024
SCARB27Dec 21, 2023
SCN10A33Nov 11, 2024
SCN11A18Nov 11, 2024
SCN1A23Nov 11, 2024
SCN1A-AS137Nov 11, 2024
SCN1B2Dec 21, 2023
SCN2A16Nov 11, 2024
SCN3A2Feb 28, 2018
SCN4A27Nov 11, 2024
SCN4B1May 26, 2021
SCN5A50Nov 11, 2024
SCN8A10Nov 11, 2024
SCN9A43Nov 11, 2024
SCNN1A1Dec 21, 2023
SCNN1B2Nov 11, 2024
SCNN1G4Nov 11, 2024
SCO12Nov 11, 2024
SCO227Nov 11, 2024
SCP214Nov 11, 2024
SCYL16Nov 11, 2024
SDCCAG81Nov 11, 2024
SDHA19Nov 11, 2024
SDHAF12Dec 21, 2023
SDHAF21Dec 21, 2023
SDHB11Nov 11, 2024
SDHC1Nov 11, 2024
SDHD4Nov 11, 2024
SEC23A1Dec 21, 2023
SEC23B27Nov 11, 2024
SEC24D2Nov 11, 2024
SEC61A11Nov 11, 2024
SEC634Nov 11, 2024
SELENON11Nov 11, 2024
SEMA3E1Jul 7, 2022
SEPT5-GP1BB3Nov 11, 2024
SEPTIN92Jan 5, 2024
SERAC17Nov 11, 2024
SERPINA112Nov 11, 2024
SERPINB61Dec 21, 2023
SERPINC122Nov 11, 2024
SERPIND13Nov 11, 2024
SERPINE11Nov 11, 2024
SERPINF12Nov 11, 2024
SERPINI11Nov 11, 2024
SETBP15Nov 11, 2024
SETD23Nov 11, 2024
SETX55Nov 11, 2024
SFXN44May 23, 2018
SGCA5Nov 11, 2024
SGCB6Nov 11, 2024
SGCD3Nov 11, 2024
SGCG4Nov 11, 2024
SGSH30Nov 11, 2024
SH2B33Nov 11, 2024
SH3BP212Nov 11, 2024
SH3KBP11Nov 11, 2024
SH3PXD2B2Feb 28, 2018
SH3TC241Nov 11, 2024
SHOC24Nov 11, 2024
SI3Nov 11, 2024
SIGMAR13Nov 11, 2024
SIK11May 26, 2021
SIL12Nov 11, 2024
SKI5Nov 11, 2024
SKIC26Jan 5, 2024
SKIC35Jan 5, 2024
SLC10A17Nov 11, 2024
SLC10A28Nov 11, 2024
SLC12A12Nov 11, 2024
SLC12A36Nov 11, 2024
SLC12A52Dec 21, 2023
SLC12A618Nov 11, 2024
SLC12A91Nov 11, 2024
SLC13A51Dec 21, 2023
SLC16A22Nov 11, 2024
SLC17A513Nov 11, 2024
SLC17A81Dec 21, 2023
SLC18A23Nov 11, 2024
SLC19A313Nov 11, 2024
SLC1A31Nov 11, 2024
SLC22A122Nov 11, 2024
SLC22A41Dec 21, 2023
SLC22A528Nov 11, 2024
SLC25A16Nov 11, 2024
SLC25A1212Dec 21, 2023
SLC25A133Dec 21, 2023
SLC25A154Nov 11, 2024
SLC25A1911Nov 11, 2024
SLC25A201May 26, 2021
SLC25A224Nov 11, 2024
SLC25A263Nov 11, 2024
SLC25A34Nov 11, 2024
SLC25A43Dec 21, 2023
SLC25A422Nov 11, 2024
SLC25A4611Nov 11, 2024
SLC26A112Nov 11, 2024
SLC26A21Feb 28, 2018
SLC26A46Nov 11, 2024
SLC26A4-AS11Dec 21, 2023
SLC26A52Dec 21, 2023
SLC26A5-AS14Jan 5, 2024
SLC27A518Nov 11, 2024
SLC29A31Nov 11, 2024
SLC2A120Nov 11, 2024
SLC2A106Nov 11, 2024
SLC2A27Dec 21, 2023
SLC2A91Dec 21, 2023
SLC30A101Nov 11, 2024
SLC33A13Dec 21, 2023
SLC34A15Dec 21, 2023
SLC34A37Nov 11, 2024
SLC35A11May 23, 2018
SLC35A22May 26, 2021
SLC35A31Dec 21, 2023
SLC35D11May 26, 2021
SLC37A44Nov 11, 2024
SLC39A1313Nov 11, 2024
SLC39A143Nov 11, 2024
SLC39A41Nov 11, 2024
SLC3A16Nov 11, 2024
SLC44A14Nov 11, 2024
SLC45A21May 23, 2018
SLC4A177Nov 11, 2024
SLC4A39Nov 11, 2024
SLC4A45Nov 11, 2024
SLC52A11Jul 7, 2022
SLC52A210Nov 11, 2024
SLC52A36Nov 11, 2024
SLC5A21Dec 21, 2023
SLC5A712Nov 11, 2024
SLC6A131Feb 28, 2018
SLC6A194Nov 11, 2024
SLC6A32Nov 11, 2024
SLC6A82Nov 11, 2024
SLC7A77Nov 11, 2024
SLC7A95Nov 8, 2024
SLC9A13Nov 11, 2024
SLC9A33Nov 11, 2024
SLC9A3-AS13Nov 11, 2024
SLC9A62Nov 11, 2024
SLFN144Nov 11, 2024
SLIT21Nov 11, 2024
SMAD37Nov 11, 2024
SMAD424Nov 11, 2024
SMAD63Nov 8, 2024
SMARCA21Dec 21, 2023
SMARCA42Nov 11, 2024
SMARCAL12Nov 11, 2024
SMARCD21Nov 11, 2024
SMC1A2Nov 11, 2024
SMCHD13Dec 21, 2023
SMPD138Nov 11, 2024
SNAP251Nov 11, 2024
SNAP297Jul 7, 2022
SNAPC51May 26, 2021
SNCA1Nov 11, 2024
SNHG142Nov 11, 2024
SNTA12Jul 7, 2022
SNX143Nov 11, 2024
SOD110Nov 11, 2024
SOD1-DT2Nov 11, 2024
SON1Feb 28, 2018
SORD7Nov 11, 2024
SOS116Nov 11, 2024
SOS22Nov 11, 2024
SOX106Nov 11, 2024
SP72Nov 11, 2024
SPARC11Nov 11, 2024
SPART6Nov 11, 2024
SPAST26Nov 11, 2024
SPEG21Nov 11, 2024
SPG1184Nov 11, 2024
SPG213Dec 21, 2023
SPG729Nov 11, 2024
SPINK110Nov 11, 2024
SPINK51Dec 21, 2023
SPMIP111Dec 21, 2023
SPR1Jan 5, 2024
SPRED11Nov 8, 2024
SPTA1184Nov 11, 2024
SPTAN113Nov 11, 2024
SPTB159Nov 11, 2024
SPTBN28Nov 11, 2024
SPTLC13May 26, 2021
SPTLC25Nov 11, 2024
SQSTM121Nov 11, 2024
SRCAP1Jul 18, 2018
SRD5A31Nov 11, 2024
SRD5A3-AS11Nov 11, 2024
SRFBP12Nov 11, 2024
SSPN1Nov 11, 2024
SSUH23May 26, 2021
ST3GAL31Nov 11, 2024
ST3GAL53Nov 11, 2024
ST6GALNAC4-ST6GALNAC6-AK12Dec 21, 2023
STAC34Nov 11, 2024
STAT15Nov 11, 2024
STAT37Nov 11, 2024
STAT5B2Nov 11, 2024
STIM14Nov 11, 2024
STING11Nov 11, 2024
STK1124Nov 11, 2024
STOM4Dec 21, 2023
STRADA2Nov 11, 2024
STRC12Nov 11, 2024
STRN41Nov 11, 2024
STUB13Nov 11, 2024
STX113Nov 11, 2024
STX1B1Jul 7, 2022
STXBP14Nov 11, 2024
STXBP213Nov 11, 2024
SUCLA212Nov 11, 2024
SUCLG18Nov 11, 2024
SUGCT18Nov 11, 2024
SUMF119Nov 11, 2024
SURF120Nov 11, 2024
SYCE21Nov 8, 2024
SYN11Dec 21, 2023
SYNE184Nov 11, 2024
SYNE41Dec 21, 2023
SYNGAP12Nov 11, 2024
SYNGAP1-AS12Nov 11, 2024
SYNJ17Nov 11, 2024
SYP2Dec 21, 2023
SYP-AS11Dec 21, 2023
SYT24Nov 11, 2024
SZT224Nov 11, 2024
SZT2-AS11Nov 11, 2024
TACO12May 23, 2018
TAF11Nov 11, 2024
TAF153Nov 11, 2024
TAFAZZIN5Jan 5, 2024
TALDO17Nov 11, 2024
TANGO21Dec 21, 2023
TAPT12Nov 11, 2024
TARID1Nov 11, 2024
TARS29May 23, 2018
TBC1D201Nov 11, 2024
TBC1D247Dec 21, 2023
TBCD3Nov 11, 2024
TBCEL-TECTA3Dec 21, 2023
TBK13Nov 11, 2024
TBX12Dec 21, 2023
TBX182Nov 11, 2024
TBX202Nov 11, 2024
TBX41Feb 28, 2018
TBX51Nov 11, 2024
TBXA2R1Nov 11, 2024
TBXAS14Nov 11, 2024
TCAP8Nov 11, 2024
TCF31Nov 11, 2024
TCF42May 26, 2021
TCN11Nov 11, 2024
TCOF13Dec 21, 2023
TCTN11Nov 8, 2024
TCTN21Nov 11, 2024
TCTN31Nov 8, 2024
TDP19Nov 11, 2024
TDP21Nov 8, 2024
TECPR217Nov 11, 2024
TECRL2Nov 11, 2024
TECTA3Dec 21, 2023
TEK4Nov 11, 2024
TENM425Nov 11, 2024
TERC7Jan 5, 2024
TERT34Nov 11, 2024
TET25Nov 11, 2024
TET2-AS15Nov 11, 2024
TFAM1Nov 11, 2024
TFG6Nov 11, 2024
TGFB23Dec 21, 2023
TGFB33Dec 21, 2023
TGFBR14Nov 11, 2024
TGFBR26Nov 11, 2024
TGM62Nov 11, 2024
TH6Nov 11, 2024
THAP12Nov 11, 2024
THAP111Jul 7, 2022
THBD27Nov 11, 2024
THG1L3Dec 21, 2023
THPO8Nov 11, 2024
TIA14Jan 5, 2024
TIMM4414May 23, 2018
TIMM8A3Nov 11, 2024
TINF25Nov 11, 2024
TJP217Nov 11, 2024
TK24Nov 11, 2024
TLR31Nov 11, 2024
TLR72Nov 11, 2024
TMC14Dec 21, 2023
TMCO62Dec 21, 2023
TMEM1071Nov 11, 2024
TMEM126A5May 23, 2018
TMEM126B2Nov 11, 2024
TMEM132E1Nov 11, 2024
TMEM1381Nov 11, 2024
TMEM2162Nov 8, 2024
TMEM2311Nov 11, 2024
TMEM38B1Nov 8, 2024
TMEM436Nov 11, 2024
TMEM6713Nov 11, 2024
TMEM7012Nov 11, 2024
TMPPE4Nov 11, 2024
TMPRSS34Dec 21, 2023
TMPRSS613Nov 11, 2024
TNC2Dec 21, 2023
TNFAIP33Nov 11, 2024
TNFRSF11A1Feb 28, 2018
TNFRSF13B4May 19, 2023
TNFRSF1A8Nov 8, 2024
TNNC13Dec 21, 2023
TNNI36Nov 11, 2024
TNNI3K6Nov 11, 2024
TNNT11Dec 21, 2023
TNNT213Nov 11, 2024
TNPO33Dec 21, 2023
TNXB95Nov 11, 2024
TOE11Oct 31, 2017
TOMT3Dec 21, 2023
TOP3A2Nov 11, 2024
TOR1A2Nov 11, 2024
TOR1AIP11Nov 11, 2024
TP5352Nov 11, 2024
TPI13Jan 5, 2024
TPK12Nov 11, 2024
TPM14Nov 8, 2024
TPM22May 26, 2021
TPM31May 23, 2022
TPM43Nov 11, 2024
TPP130Nov 11, 2024
TPP23Nov 11, 2024
TPRN4Nov 11, 2024
TRAF3IP14Nov 11, 2024
TRAP118May 23, 2018
TRAPPC115Nov 11, 2024
TRAPPC92Feb 28, 2018
TRB10Nov 11, 2024
TRDN9Nov 11, 2024
TREM23Nov 11, 2024
TREX16Nov 11, 2024
TRIM26Nov 11, 2024
TRIM329Nov 11, 2024
TRIM3711Nov 8, 2024
TRIM59-IFT801Nov 11, 2024
TRIM633Nov 11, 2024
TRIOBP11Nov 11, 2024
TRIP111Oct 17, 2022
TRIP45Nov 11, 2024
TRMT10C1Nov 8, 2024
TRMU13Nov 11, 2024
TRNT13Nov 11, 2024
TRPA11May 26, 2021
TRPC62Nov 11, 2024
TRPM62Dec 21, 2023
TRPV420Nov 11, 2024
TSC116Nov 11, 2024
TSC243Nov 11, 2024
TSFM8Nov 11, 2024
TSPAN110Nov 11, 2024
TTBK21Nov 11, 2024
TTC142Nov 11, 2024
TTC1911Nov 11, 2024
TTC21B8Nov 11, 2024
TTC7A10Nov 11, 2024
TTC81Nov 11, 2024
TTN706Nov 11, 2024
TTN-AS1442Nov 11, 2024
TTPA7Nov 11, 2024
TTR22Nov 11, 2024
TUBA1A1Jul 18, 2018
TUBA4A2Nov 11, 2024
TUBA84Dec 21, 2023
TUBB111Nov 11, 2024
TUBB32Jul 7, 2022
TUBB63Nov 11, 2024
TUFM4Nov 11, 2024
TUSC31Feb 28, 2018
TWNK30Nov 11, 2024
TYK22Nov 11, 2024
TYMP34Nov 11, 2024
TYROBP2Nov 11, 2024
UBA12Nov 11, 2024
UBA52Nov 11, 2024
UBE3A2Nov 11, 2024
UBQLN22Dec 21, 2023
UCHL11Nov 11, 2024
UGT1A20May 31, 2024
UGT1A120May 31, 2024
UGT1A1020May 31, 2024
UGT1A320May 31, 2024
UGT1A420May 31, 2024
UGT1A520May 31, 2024
UGT1A620May 31, 2024
UGT1A720May 31, 2024
UGT1A820May 31, 2024
UGT1A920May 31, 2024
UMOD7Nov 11, 2024
UNC13A2Nov 11, 2024
UNC13D14Nov 11, 2024
UNC45A6Nov 11, 2024
UNG1Jul 7, 2022
UPF3B1Feb 28, 2018
UQCRB1May 23, 2018
UQCRC27Nov 11, 2024
UQCRQ1May 23, 2018
UROD17Nov 11, 2024
UROS3Nov 11, 2024
USB112Jan 5, 2024
USH1C1Dec 21, 2023
USH1G2Dec 21, 2023
USH2A13Nov 11, 2024
USH2A-AS12Dec 21, 2023
USP72Nov 11, 2024
USP7-AS11Dec 21, 2023
USP9X3Jul 18, 2018
VARS244Nov 11, 2024
VAV11Feb 28, 2018
VCL12Nov 11, 2024
VCP7Nov 11, 2024
VDR3Nov 11, 2024
VEPH11Feb 28, 2018
VHL8Nov 11, 2024
VIPAS395Nov 11, 2024
VKORC11Nov 8, 2024
VLDLR7Nov 11, 2024
VPS13A14Nov 11, 2024
VPS13A-AS11Nov 11, 2024
VPS13B34Nov 11, 2024
VPS13C26Nov 11, 2024
VPS13D52Nov 11, 2024
VPS33A2Nov 11, 2024
VPS33B16Nov 11, 2024
VPS353Nov 11, 2024
VPS37A4Dec 21, 2023
VPS458Nov 11, 2024
VRK15Nov 11, 2024
VWA13Nov 11, 2024
VWF105Nov 11, 2024
WARS12Nov 11, 2024
WAS10Nov 11, 2024
WASHC517Nov 11, 2024
WASHC5-AS12Nov 11, 2024
WDR12Nov 11, 2024
WDR193Nov 11, 2024
WDR261Dec 21, 2023
WDR352Nov 11, 2024
WDR451Nov 11, 2024
WDR6221Nov 11, 2024
WDR721Nov 11, 2024
WDR733Nov 11, 2024
WDR8113Nov 11, 2024
WFS116Nov 11, 2024
WHRN3Nov 11, 2024
WIPF110Nov 11, 2024
WNK136Nov 11, 2024
WRAP535Nov 11, 2024
WRN8Nov 11, 2024
WWOX9Dec 21, 2023
XDH6Nov 11, 2024
XIAP4Nov 11, 2024
XPA5Dec 21, 2023
XPC10Dec 21, 2023
XPNPEP35Nov 11, 2024
XPR11Nov 11, 2024
XYLT14Dec 21, 2023
XYLT21Nov 11, 2024
YARS15Nov 11, 2024
YARS211Nov 11, 2024
ZAP706Dec 21, 2023
ZBTB181Feb 28, 2018
ZC4H21Feb 28, 2018
ZCCHC81Nov 11, 2024
ZDHHC242Nov 8, 2024
ZEB23Dec 21, 2023
ZFYVE2649Nov 11, 2024
ZMPSTE242Nov 11, 2024
ZMYND101Nov 11, 2024
ZNF1481Feb 28, 2018
ZNF27610Jan 5, 2024
ZNF4233Nov 11, 2024
ZNF46954Nov 11, 2024
ZNF518A1May 26, 2021
ZRANB31Nov 11, 2024

Condition

NameSubmissionsLast Updated
3-methylglutaconic aciduria type 12Feb 28, 2018
3MC syndrome 11Feb 28, 2018
4p partial monosomy syndrome1Feb 28, 2018
AHDC1-related intellectual disability - obstructive sleep apnea - mild dysmorphism syndrome1Feb 28, 2018
ALG12-congenital disorder of glycosylation1Feb 28, 2018
ALG8 congenital disorder of glycosylation2Feb 28, 2018
Aarskog syndrome1Feb 28, 2018
Achondrogenesis type II1Feb 28, 2018
Acyl-CoA oxidase deficiency1Feb 28, 2018
Adenylosuccinate lyase deficiency1Feb 28, 2018
Adrenoleukodystrophy3Jul 18, 2018
Adult polyglucosan body disease1Feb 28, 2018
Agammaglobulinemia 2, autosomal recessive1Feb 28, 2018
Aicardi-Goutieres syndrome 61Feb 28, 2018
Aicardi-Goutieres syndrome 71Feb 28, 2018
Aminoacylase 1 deficiency1Feb 28, 2018
Arrhythmogenic right ventricular dysplasia 21Feb 28, 2018
Arterial calcification, generalized, of infancy, 12Feb 28, 2018
Arthrogryposis, distal, with impaired proprioception and touch3Feb 28, 2018
Aspartylglucosaminuria1Feb 28, 2018
Ataxia-hypogonadism-choroidal dystrophy syndrome1Feb 28, 2018
Ataxia-telangiectasia syndrome1Jul 18, 2018
Atrial septal defect 71Feb 28, 2018
Autism spectrum disorder due to AUTS2 deficiency1Feb 28, 2018
Autosomal dominant Charcot-Marie-Tooth disease type 2W1Feb 28, 2018
Autosomal dominant centronuclear myopathy1Jul 18, 2018
Autosomal dominant cerebellar ataxia, deafness and narcolepsy1Feb 28, 2018
Autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures1Feb 28, 2018
Autosomal dominant nonsyndromic hearing loss 111Feb 28, 2018
Autosomal recessive Parkinson disease 141Oct 26, 2023
Autosomal recessive Robinow syndrome1Feb 28, 2018
Autosomal recessive ataxia due to ubiquinone deficiency1Feb 28, 2018
Autosomal recessive ataxia, Beauce type1Feb 28, 2018
Autosomal recessive early-onset Parkinson disease 231Feb 28, 2018
Autosomal recessive hypophosphatemic bone disease1Jul 18, 2018
Autosomal recessive limb-girdle muscular dystrophy type 2G1Feb 28, 2018
Autosomal recessive limb-girdle muscular dystrophy type 2J2Feb 28, 2018
Autosomal recessive limb-girdle muscular dystrophy type 2Q1Feb 28, 2018
Autosomal recessive multiple pterygium syndrome1Feb 28, 2018
Autosomal recessive nonsyndromic hearing loss 281Feb 28, 2018
Autosomal recessive nonsyndromic hearing loss 771Feb 28, 2018
Autosomal recessive polycystic kidney disease1Feb 28, 2018
Autosomal recessive spinocerebellar ataxia 141Feb 28, 2018
Avascular necrosis of femoral head, primary, 11Feb 28, 2018
BENTA disease1Jul 18, 2018
Bardet-Biedl syndrome 11Feb 28, 2018
Bardet-Biedl syndrome 111Feb 28, 2018
Bethlem myopathy 1A2Feb 28, 2018
Biotin-responsive basal ganglia disease1Feb 28, 2018
Bloom syndrome2Jul 18, 2018
Bosch-Boonstra-Schaaf optic atrophy syndrome2Feb 28, 2018
CBL-related disorder1Feb 28, 2018
CODAS syndrome1Feb 28, 2018
Catecholaminergic polymorphic ventricular tachycardia 11Feb 28, 2018
Central core myopathy1Feb 28, 2018
Cerebellar ataxia, intellectual disability, and dysequilibrium syndrome 21Feb 28, 2018
Cerebellar ataxia, intellectual disability, and dysequilibrium syndrome 41Feb 28, 2018
Cerebroretinal microangiopathy with calcifications and cysts 12Jul 18, 2018
Charcot-Marie-Tooth disease axonal type 2O1Feb 28, 2018
Charcot-Marie-Tooth disease dominant intermediate B1Jul 18, 2018
Charcot-Marie-Tooth disease type 2B11Jul 18, 2018
Charcot-Marie-Tooth disease type 2D1Feb 28, 2018
Charcot-Marie-Tooth disease type 4F1Feb 28, 2018
Charlevoix-Saguenay spastic ataxia1Jul 18, 2018
Ciliary dyskinesia, primary, 36, X-linked1Jul 18, 2018
Classic dopamine transporter deficiency syndrome1Feb 28, 2018
Coffin-Lowry syndrome1Feb 28, 2018
Cohen syndrome1Feb 28, 2018
Combined immunodeficiency due to LRBA deficiency3Feb 28, 2018
Combined immunodeficiency due to MALT1 deficiency1Feb 28, 2018
Combined malonic and methylmalonic acidemia2Feb 28, 2018
Combined oxidative phosphorylation defect type 151Feb 28, 2018
Combined oxidative phosphorylation defect type 71Feb 28, 2018
Combined oxidative phosphorylation deficiency 191Feb 28, 2018
Complement component 5 deficiency1Feb 28, 2018
Cone-rod dystrophy 151Feb 28, 2018
Cone-rod dystrophy 51Feb 28, 2018
Congenital afibrinogenemia2Feb 28, 2018
Congenital bile acid synthesis defect 61Jul 18, 2018
Congenital diarrhea 7 with exudative enteropathy1Feb 28, 2018
Congenital heart defects, multiple types, 41Feb 28, 2018
Congenital muscular dystrophy due to LMNA mutation1Jul 18, 2018
Congenital muscular dystrophy due to integrin alpha-7 deficiency1Feb 28, 2018
Congenital muscular hypertrophy-cerebral syndrome1Feb 28, 2018
Congenital myasthenic syndrome 102Feb 28, 2018
Congenital myasthenic syndrome 111Feb 28, 2018
Congenital myasthenic syndrome 131Feb 28, 2018
Congenital myasthenic syndrome 52Feb 28, 2018
Congenital myasthenic syndrome 81Feb 28, 2018
Congenital myotonia, autosomal recessive form2Feb 28, 2018
Congenital secretory sodium diarrhea 81Feb 28, 2018
Corneal dystrophy, Fuchs endothelial, 31Jul 18, 2018
Curry-Hall syndrome1Feb 28, 2018
Cutis laxa, autosomal dominant 11Feb 28, 2018
DPAGT1-congenital disorder of glycosylation1Feb 28, 2018
Deficiency of alpha-mannosidase2Feb 28, 2018
Dejerine-Sottas disease1Feb 28, 2018
Dermatitis, atopic, 22Feb 28, 2018
Developmental and epileptic encephalopathy 941Feb 28, 2018
Developmental and epileptic encephalopathy, 112Jul 18, 2018
Developmental and epileptic encephalopathy, 131Feb 28, 2018
Developmental and epileptic encephalopathy, 162Feb 28, 2018
Developmental and epileptic encephalopathy, 271Jul 18, 2018
Developmental and epileptic encephalopathy, 421Jul 16, 2018
Developmental and epileptic encephalopathy, 72Feb 28, 2018
Developmental delay with autism spectrum disorder and gait instability2Jul 18, 2018
Dilated cardiomyopathy 1A1Jul 18, 2018
Dilated cardiomyopathy 1DD1Feb 28, 2018
Dilated cardiomyopathy 1G1Feb 28, 2018
Dilated cardiomyopathy 1O1Feb 28, 2018
Dilated cardiomyopathy 1S2Feb 28, 2018
Dilated cardiomyopathy 3B1Feb 28, 2018
Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome1Jul 18, 2018
Distichiasis-lymphedema syndrome1Feb 28, 2018
Dyskeratosis congenita, autosomal dominant 21Feb 28, 2018
Dystonia 28, childhood-onset1Jul 18, 2018
Ehlers-Danlos syndrome, classic type2Jul 16, 2018
Ehlers-Danlos syndrome, type 41Mar 9, 2022
Ellis-van Creveld syndrome1Feb 28, 2018
Emery-Dreifuss muscular dystrophy 2, autosomal dominant1Jul 18, 2018
Emery-Dreifuss muscular dystrophy 3, autosomal recessive1Jul 18, 2018
Epilepsy, childhood absence, susceptibility to, 51Feb 28, 2018
Epilepsy, childhood absence, susceptibility to, 62Feb 28, 2018
Epilepsy, familial adult myoclonic, 51Feb 28, 2018
Epilepsy, familial focal, with variable foci 11Feb 28, 2018
Epilepsy, familial temporal lobe, 11Feb 28, 2018
Epilepsy, idiopathic generalized, susceptibility to, 121Feb 28, 2018
Epilepsy, idiopathic generalized, susceptibility to, 92Jul 18, 2018
Epiphyseal dysplasia, multiple, 21Feb 28, 2018
Epiphyseal dysplasia, multiple, 61Feb 28, 2018
Episodic ataxia type 22Jul 18, 2018
Episodic ataxia type 51Jul 18, 2018
Familial Mediterranean fever1Feb 28, 2018
Familial cold autoinflammatory syndrome 21Feb 28, 2018
Familial cold autoinflammatory syndrome 42Feb 28, 2018
Familial expansile osteolysis1Feb 28, 2018
Familial infantile myasthenia2Feb 28, 2018
Familial infantile myoclonic epilepsy1Feb 28, 2018
Familial partial lipodystrophy, Dunnigan type1Jul 18, 2018
Familial temporal lobe epilepsy 72Feb 28, 2018
Fetal akinesia deformation sequence 11Feb 28, 2018
Fetal akinesia-cerebral and retinal hemorrhage syndrome1Jul 18, 2018
Floating-Harbor syndrome1Jul 18, 2018
Frank-Ter Haar syndrome2Feb 28, 2018
Fraser syndrome 12Mar 18, 2024
Global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies1Feb 28, 2018
Glycogen storage disease due to phosphoglycerate kinase 1 deficiency1Feb 28, 2018
Glycogen storage disease, type II1Feb 28, 2018
Glycogen storage disease, type IV1Feb 28, 2018
Gorlin syndrome1Feb 28, 2018
Growth delay due to insulin-like growth factor I resistance1Feb 28, 2018
Heart-hand syndrome, Slovenian type1Jul 18, 2018
Heimler syndrome 11Feb 28, 2018
Hereditary sensory neuropathy-deafness-dementia syndrome1Feb 28, 2018
Hereditary spastic paraplegia 151Nov 19, 2019
Hereditary spastic paraplegia 21Jul 18, 2018
Hereditary spastic paraplegia 353Feb 28, 2018
Hereditary spastic paraplegia 391Feb 28, 2018
Hereditary spastic paraplegia 551Feb 28, 2018
Hereditary spastic paraplegia 641Feb 28, 2018
Hereditary spastic paraplegia 71Jul 18, 2018
Heterotopia, periventricular, X-linked dominant1Feb 28, 2018
Holocarboxylase synthetase deficiency1Feb 28, 2018
Hutchinson-Gilford syndrome1Jul 18, 2018
Hypercholesterolemia, familial, 15May 27, 2021
Hyperinsulinemic hypoglycemia, familial, 11Feb 28, 2018
Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome1Feb 28, 2018
Hyperphosphatasia with intellectual disability syndrome 12Feb 28, 2018
Hyperphosphatasia with intellectual disability syndrome 41Feb 28, 2018
Hypertrophic cardiomyopathy 251Feb 28, 2018
Hypophosphatemic rickets, autosomal recessive, 22Feb 28, 2018
Hypotonia, ataxia, and delayed development syndrome1Feb 28, 2018
Ichthyosis vulgaris2Feb 28, 2018
Immunodeficiency 11b with atopic dermatitis1Jul 18, 2018
Immunodeficiency due to MASP-2 deficiency1Feb 28, 2018
Infantile cerebellar-retinal degeneration2Jul 18, 2018
Infantile neuroaxonal dystrophy2Oct 26, 2023
Intellectual disability, X-linked 1021Feb 28, 2018
Intellectual disability, X-linked 191Feb 28, 2018
Intellectual disability, X-linked 992Jul 18, 2018
Intellectual disability, X-linked 99, syndromic, female-restricted1Feb 28, 2018
Intellectual disability, X-linked syndromic, Turner type1Feb 28, 2018
Intellectual disability, autosomal dominant 11Apr 22, 2024
Intellectual disability, autosomal dominant 131Feb 28, 2018
Intellectual disability, autosomal dominant 221Feb 28, 2018
Intellectual disability, autosomal dominant 51Feb 28, 2018
Intellectual disability, autosomal dominant 61Jul 18, 2018
Intellectual disability, autosomal recessive 132Feb 28, 2018
Intellectual disability, autosomal recessive 181Feb 28, 2018
Intellectual disability, autosomal recessive 462Feb 28, 2018
Intellectual disability, autosomal recessive 71Feb 28, 2018
Intellectual disability-feeding difficulties-developmental delay-microcephaly syndrome1Jul 18, 2018
Intellectual disability-hypotonia-spasticity-sleep disorder syndrome1Feb 28, 2018
Joubert syndrome 232Feb 28, 2018
Joubert syndrome 51Feb 28, 2018
Juvenile myelomonocytic leukemia1Feb 28, 2018
KBG syndrome2Feb 28, 2018
Kabuki syndrome 11Feb 28, 2018
Klippel-Feil anomaly-myopathy-facial dysmorphism syndrome1Feb 28, 2018
Kniest dysplasia1Feb 28, 2018
Koolen-de Vries syndrome1Feb 28, 2018
Landau-Kleffner syndrome1Feb 28, 2018
Laron-type isolated somatotropin defect1Feb 28, 2018
Larsen-like syndrome, B3GAT3 type1Feb 28, 2018
Laurence-Moon syndrome1Feb 28, 2018
Legg-Calve-Perthes disease1Feb 28, 2018
Leigh syndrome1Feb 28, 2018
Lethal multiple pterygium syndrome1Feb 28, 2018
Lethal tight skin contracture syndrome1Jul 18, 2018
Lissencephaly due to TUBA1A mutation1Jul 18, 2018
Lissencephaly type 1 due to doublecortin gene mutation1Feb 28, 2018
Loeys-Dietz syndrome 21Feb 28, 2018
MASA syndrome1Feb 28, 2018
Macrocephaly, dysmorphic facies, and psychomotor retardation2Feb 28, 2018
Macular corneal dystrophy1Feb 28, 2018
Mandibuloacral dysplasia with type A lipodystrophy1Jul 18, 2018
Marfan syndrome1May 27, 2021
Mastocytosis1Feb 28, 2018
Mayer-Rokitansky-Kuster-Hauser syndrome1Feb 28, 2018
Megaconial type congenital muscular dystrophy1Feb 28, 2018
Megalencephalic leukoencephalopathy with subcortical cysts 11Feb 28, 2018
Meier-Gorlin syndrome 11Feb 28, 2018
Merosin deficient congenital muscular dystrophy2Feb 28, 2018
Methylmalonic acidemia with homocystinuria, type cblX1Feb 28, 2018
Microcephaly 1, primary, autosomal recessive1Feb 28, 2018
Microcephaly 3, primary, autosomal recessive3Feb 28, 2018
Microcephaly 5, primary, autosomal recessive2Feb 28, 2018
Microcephaly with or without chorioretinopathy, lymphedema, or intellectual disability1Feb 28, 2018
Mitochondrial DNA depletion syndrome 12B (cardiomyopathic type), autosomal recessive1Jul 18, 2018
Mitochondrial DNA depletion syndrome 4b1Feb 28, 2018
Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)1Feb 28, 2018
Mitochondrial DNA depletion syndrome, myopathic form1Feb 28, 2018
Mitochondrial complex I deficiency3Jul 18, 2018
Mitochondrial complex III deficiency nuclear type 21Feb 28, 2018
Mitochondrial complex IV deficiency, nuclear type 11Feb 28, 2018
Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency2Feb 28, 2018
Mitochondrial trifunctional protein deficiency1Feb 28, 2018
Mucopolysaccharidosis type 61Feb 28, 2018
Mucopolysaccharidosis, MPS-III-A1Feb 28, 2018
Multiple acyl-CoA dehydrogenase deficiency1Feb 28, 2018
Multiple congenital anomalies-hypotonia-seizures syndrome 11Jul 18, 2018
Multiple congenital anomalies-hypotonia-seizures syndrome 31Feb 28, 2018
Multiple epiphyseal dysplasia type 41Feb 28, 2018
Multiple epiphyseal dysplasia, Beighton type1Feb 28, 2018
Multiple gastrointestinal atresias1Feb 28, 2018
Muscle AMP deaminase deficiency2Feb 28, 2018
Myeloid neoplasm1Oct 17, 2022
Myopathy due to calsequestrin and SERCA1 protein overload1Feb 28, 2018
Myopathy, centronuclear, 21Feb 28, 2018
Myopia, high, with cataract and vitreoretinal degeneration1Feb 28, 2018
Namaqualand hip dysplasia1Feb 28, 2018
Nemaline myopathy 24Feb 28, 2018
Neurodegeneration with brain iron accumulation 2B1Oct 26, 2023
Neuronopathy, distal hereditary motor, type 5A1Feb 28, 2018
Niemann-Pick disease, type C12Feb 28, 2018
Norman-Roberts syndrome1Feb 28, 2018
Occipital pachygyria and polymicrogyria1Feb 28, 2018
Otospondylomegaepiphyseal dysplasia, autosomal dominant1Feb 28, 2018
Paget disease of bone 2, early-onset1Feb 28, 2018
Paroxysmal nocturnal hemoglobinuria 21Feb 28, 2018
Pelizaeus-Merzbacher disease1Jul 18, 2018
Periodic fever-infantile enterocolitis-autoinflammatory syndrome2Feb 28, 2018
Peroxisome biogenesis disorder 1A (Zellweger)1Feb 28, 2018
Peroxisome biogenesis disorder 1B2Feb 28, 2018
Peroxisome biogenesis disorder 2A (Zellweger)1Feb 28, 2018
Peroxisome biogenesis disorder 2B1Feb 28, 2018
Peroxisome biogenesis disorder 5A (Zellweger)2Feb 28, 2018
Peroxisome biogenesis disorder 5B2Feb 28, 2018
Peters plus syndrome1Feb 28, 2018
Phenylketonuria1Feb 28, 2018
Pitt-Hopkins syndrome1Jul 18, 2018
Pitt-Hopkins-like syndrome 21Feb 28, 2018
Platyspondylic dysplasia, Torrance type1Feb 28, 2018
Primary ciliary dyskinesia 131Feb 28, 2018
Primary ciliary dyskinesia 171Feb 28, 2018
Primary ciliary dyskinesia 211Feb 28, 2018
Primary ciliary dyskinesia 291Mar 20, 2024
Primary ciliary dyskinesia 34Feb 28, 2018
Primary ciliary dyskinesia 51Feb 28, 2018
Primary ciliary dyskinesia 71Feb 28, 2018
Primary ciliary dyskinesia 91Jul 16, 2018
Progressive sclerosing poliodystrophy2Feb 28, 2018
Proline dehydrogenase deficiency2Feb 28, 2018
Pulmonary hypertension, primary, 41Feb 28, 2018
Pyruvate dehydrogenase E2 deficiency2Feb 28, 2018
RFT1-congenital disorder of glycosylation1Feb 28, 2018
Rafiq syndrome1Feb 28, 2018
Renal carnitine transport defect1Feb 28, 2018
Rett syndrome2Jul 18, 2018
Rhizomelic chondrodysplasia punctata type 51Feb 28, 2018
Sarcotubular myopathy1Feb 28, 2018
Schwartz-Jampel syndrome2Jul 18, 2018
Seizures, benign familial infantile, 32Jul 18, 2018
Seizures, benign familial infantile, 51Feb 28, 2018
Seizures, benign familial neonatal, 12Feb 28, 2018
Seizures, benign familial neonatal, 21Feb 28, 2018
Seizures-scoliosis-macrocephaly syndrome2Feb 28, 2018
Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis2Jul 18, 2018
Severe combined immunodeficiency due to CARD11 deficiency1Jul 18, 2018
Severe combined immunodeficiency due to IKK2 deficiency2Feb 28, 2018
Severe feeding difficulties-failure to thrive-microcephaly due to ASXL3 deficiency syndrome1Feb 28, 2018
Severe intellectual disability-progressive spastic diplegia syndrome1Jul 18, 2018
Short stature due to partial GHR deficiency2Feb 28, 2018
Singleton-Merten syndrome 11Feb 28, 2018
Spastic ataxia 51Feb 28, 2018
Spinocerebellar ataxia type 281Feb 28, 2018
Spinocerebellar ataxia type 51Feb 28, 2018
Spondyloepimetaphyseal dysplasia with multiple dislocations1Feb 28, 2018
Spondyloepiphyseal dysplasia congenita1Feb 28, 2018
Spondyloepiphyseal dysplasia with metatarsal shortening1Feb 28, 2018
Spondyloepiphyseal dysplasia, Stanescu type1Feb 28, 2018
Spondylometaphyseal dysplasia1Feb 28, 2018
Spondyloperipheral dysplasia1Feb 28, 2018
Steel syndrome1Feb 28, 2018
Stickler syndrome type 11Feb 28, 2018
Stickler syndrome, type 41Feb 28, 2018
Stickler syndrome, type 51Feb 28, 2018
Stickler syndrome, type I, nonsyndromic ocular1Feb 28, 2018
Supravalvar aortic stenosis1Feb 28, 2018
Symmetrical dyschromatosis of extremities1Feb 28, 2018
Syndromic X-linked intellectual disability 141Feb 28, 2018
Tay-Sachs disease1Jul 18, 2018
Telangiectasia, hereditary hemorrhagic, type 14May 27, 2021
Temtamy syndrome1Feb 28, 2018
Thyroglobulin synthesis defect1Feb 28, 2018
Thyroid dyshormonogenesis 61Feb 28, 2018
Torsion dystonia 61Feb 28, 2018
Trichomegaly-retina pigmentary degeneration-dwarfism syndrome1Feb 28, 2018
Tuberous sclerosis 21Feb 28, 2018
Ullrich congenital muscular dystrophy 1A2Feb 28, 2018
Urofacial syndrome type 11Feb 28, 2018
Usher syndrome type 1G1Feb 28, 2018
Usher syndrome type 2A1Jul 18, 2018
Usher syndrome type 3B1Feb 28, 2018
Ventricular septal defect 31Feb 28, 2018
Waardenburg syndrome type 4A1Feb 28, 2018
Wieacker-Wolff syndrome1Feb 28, 2018
X-linked agammaglobulinemia1Feb 28, 2018
X-linked agammaglobulinemia with growth hormone deficiency1Feb 28, 2018
X-linked chondrodysplasia punctata 11Feb 28, 2018
X-linked intellectual disability-psychosis-macroorchidism syndrome1Feb 28, 2018
ZTTK syndrome1Feb 28, 2018
not provided18602Nov 11, 2024
not specified452Jul 25, 2024

Testing in GTR

Disease nameNumber of tests
2-hydroxyglutaric aciduria1 test
3-Methylglutaconic aciduria1 test
3-Methylglutaconic aciduria type 21 test
3-methylglutaconic aciduria type 53 tests
3-methylglutaconic aciduria, type VIIA1 test
3-methylglutaconic aciduria, type VIIB1 test
46,XX testicular disorder of sex development1 test
46,xx gonadal dysgenesis, complete, sry-positive1 test
ALG1-congenital disorder of glycosylation1 test
ALPI-related inflammatory bowel disease1 test
Abacavir hypersensitivity1 test
Abetalipoproteinaemia1 test
Acid sphingomyelinase deficiency1 test
Acrodysostosis with multiple hormone resistance1 test
Acromicric dysplasia4 tests
Activated PI3K-delta syndrome2 tests
Acute febrile neutrophilic dermatosis2 tests
Acute intermittent porphyria8 tests
Acute myeloid leukemia3 tests
Adams-Oliver syndrome3 tests
Adenine phosphoribosyltransferase deficiency1 test
Adrenoleukodystrophy4 tests
Adrenomyeloneuropathy2 tests
Adult Krabbe disease1 test
Adult hypophosphatasia1 test
Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy1 test
Agammaglobulinemia2 tests
Agammaglobulinemia 2, autosomal recessive1 test
Agammaglobulinemia 3, autosomal recessive1 test
Agammaglobulinemia 4, autosomal recessive1 test
Agammaglobulinemia 6, autosomal recessive1 test
Agammaglobulinemia 7, autosomal recessive1 test
Agammaglobulinemia 8, autosomal dominant1 test
Agammaglobulinemia 8b, autosomal recessive1 test
Aganglionic megacolon1 test
Aicardi Goutieres syndrome2 tests
Aicardi-Goutieres syndrome 11 test
Aicardi-Goutieres syndrome 1, autosomal dominant1 test
Aicardi-Goutieres syndrome 21 test
Aicardi-Goutieres syndrome 31 test
Aicardi-Goutieres syndrome 41 test
Aicardi-Goutieres syndrome 51 test
Aicardi-Goutieres syndrome 61 test
Aicardi-Goutieres syndrome 73 tests
Aicardi-Goutieres syndrome 81 test
Aicardi-Goutieres syndrome 91 test
Alagille syndrome due to a JAG1 point mutation4 tests
Alagille syndrome due to a NOTCH2 point mutation4 tests
Alkaptonuria1 test
Allopurinol response1 test
Alpha-1-antitrypsin deficiency1 test
Alport syndrome2 tests
Alstrom syndrome3 tests
Alzheimer disease 21 test
Ambiguous genitalia1 test
Amelogenesis imperfecta type 1G1 test
Amyloidosis, hereditary systemic 15 tests
Amyotrophic lateral sclerosis2 tests
Amyotrophic lateral sclerosis type 11 test
Amyotrophic neuralgia1 test
Anauxetic dysplasia 11 test
Andersen Tawil syndrome5 tests
Anemia, nonspherocytic hemolytic, due to G6PD deficiency3 tests
Angelman syndrome1 test
Angelman syndrome due to paternal uniparental disomy of chromosome 151 test
Anomaly of sex chromosome4 tests
Antenatal Bartter syndrome1 test
Aplastic anemia4 tests
Arginine:glycine amidinotransferase deficiency3 tests
Arrhythmogenic cardiomyopathy7 tests
Arrhythmogenic cardiomyopathy with wooly hair and keratoderma4 tests
Arrhythmogenic right ventricular cardiomyopathy7 tests
Arterial tortuosity syndrome3 tests
Arylsulfatase A pseudodeficiency1 test
Asperger syndrome1 test
Ataxia-pancytopenia syndrome1 test
Ataxia-telangiectasia syndrome2 tests
Atazanavir response2 tests
Athabaskan severe combined immunodeficiency2 tests
Atomoxetine response1 test
Atorvastatin response1 test
Atrial fibrillation7 tests
Atypical hemolytic-uremic syndrome1 test
Atypical hemolytic-uremic syndrome with thrombomodulin anomaly1 test
Autism spectrum disorder2 tests
Autoimmune disease1 test
Autoimmune disease, multisystem, infantile-onset2 tests
Autoimmune disease, multisystem, infantile-onset, 23 tests
Autoimmune enteropathy and endocrinopathy - susceptibility to chronic infections syndrome1 test
Autoimmune interstitial lung disease-arthritis syndrome1 test
Autoimmune lymphoproliferative syndrome3 tests
Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsufficiency5 tests
Autoimmune lymphoproliferative syndrome type 11 test
Autoimmune lymphoproliferative syndrome type 1, autosomal recessive1 test
Autoimmune lymphoproliferative syndrome type 2A3 tests
Autoimmune lymphoproliferative syndrome type 2B2 tests
Autoimmune lymphoproliferative syndrome, type 1a1 test
Autoimmune lymphoproliferative syndrome, type 1b2 tests
Autoimmune lymphoproliferative syndrome, type III caused by mutation in PRKCD6 tests
Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia1 test
Autoimmune polyglandular syndrome type 1, autosomal dominant1 test
Autoimmune polyglandular syndrome type 1, with reversible metaphyseal dysplasia2 tests
Autoinflammation with arthritis and dyskeratosis1 test
Autoinflammation with episodic fever and lymphadenopathy3 tests
Autoinflammation, immune dysregulation, and eosinophilia3 tests
Autoinflammation-PLCG2-associated antibody deficiency-immune dysregulation3 tests
Autoinflammatory disease, X-linked2 tests
Autoinflammatory disease, systemic, with vasculitis1 test
Autoinflammatory syndrome2 tests
Autoinflammatory syndrome, familial, Behcet-like2 tests
Autoinflammatory syndrome, familial, Behcet-like 13 tests
Autoinflammatory-pancytopenia syndrome due to DNASE2 deficiency1 test
Autosomal chromosomal disorder6 tests
Autosomal dominant distal myopathy1 test
Autosomal dominant hypocalcemia2 tests
Autosomal dominant hypocalcemia 21 test
Autosomal dominant medullary cystic kidney disease with or without hyperuricemia1 test
Autosomal dominant polycystic kidney disease2 tests
Autosomal dominant polycystic liver disease1 test
Autosomal recessive agammaglobulinemia 11 test
Autosomal recessive dyskeratosis congenita 42 tests
Autosomal recessive familial Mediterranean fever2 tests
Autosomal recessive polycystic kidney disease1 test
Autosomal recessive severe congenital neutropenia due to CSF3R deficiency1 test
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency2 tests
Autosomal recessive severe congenital neutropenia due to JAGN1 deficiency1 test
Autosomal recessive spinocerebellar ataxia 141 test
Autosomal systemic lupus erythematosus type 161 test
Autosomal uniparental disomy1 test
Azathioprine response1 test
Azorean disease1 test
B-cell immunodeficiency, distal limb anomalies, and urogenital malformations1 test
BAP1-related tumor predisposition syndrome1 test
BENTA disease2 tests
Baraitser-Winter syndrome2 tests
Bare lymphocyte syndrome type 2, complementation group A1 test
Bartter disease type 12 tests
Bartter disease type 22 tests
Bartter disease type 32 tests
Bartter disease type 4A2 tests
Bartter disease type 4B2 tests
Bartter disease type 52 tests
Bartter syndrome3 tests
Bartter syndrome with hypocalcemia1 test
Batten-Turner congenital myopathy1 test
Becker muscular dystrophy5 tests
Beckwith-Wiedemann syndrome2 tests
Belinostat response2 tests
Berardinelli-Seip congenital lipodystrophy1 test
Beta-thalassemia and related diseases1 test
Bethlem myopathy2 tests
Bile acid malabsorption, primary, 11 test
Bile acid malabsorption, primary, 21 test
Biotinidase deficiency1 test
Birt-Hogg-Dube syndrome1 test
Blau syndrome1 test
Blepharophimosis - intellectual disability syndrome, Ohdo type2 tests
Bone marrow failure syndrome 31 test
Branchial arch or oral-acral syndrome1 test
Breast cancer, susceptibility to1 test
Brittle cornea syndrome2 tests
Bruck syndrome1 test
Brugada syndrome6 tests
Bupropion response1 test
C1Q deficiency1 test
C1Q deficiency 21 test
C1Q deficiency 31 test
CARASIL syndrome1 test
CHARGE syndrome2 tests
COL4A1 or COL4A2-related cerebral small vessel disease2 tests
Candidiasis, familial, 61 test
Candidiasis, familial, 81 test
Candidiasis, familial, 91 test
Capecitabine response2 tests
Capillary malformation-arteriovenous malformation syndrome2 tests
Carbamazepine hypersensitivity1 test
Carbamazepine response1 test
Carcinoid syndrome2 tests
Cardiac arrhythmia9 tests
Cardiac valvular dysplasia, X-linked3 tests
Cardiofaciocutaneous syndrome 15 tests
Cardiofaciocutaneous syndrome 25 tests
Cardiofaciocutaneous syndrome 35 tests
Cardiofaciocutaneous syndrome 45 tests
Cardiomyopathy8 tests
Cardiomyopathy, dilated, with wooly hair, keratoderma, and tooth agenesis5 tests
Carney complex1 test
Carnitine acylcarnitine translocase deficiency1 test
Carnitine palmitoyl transferase II deficiency, severe infantile form1 test
Carnitine palmitoyltransferase II deficiency4 tests
Catechol-o-methyltransferase deficiency1 test
Catecholaminergic polymorphic ventricular tachycardia 17 tests
Cerebral amyloid angiopathy1 test
Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 11 test
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy1 test
Cerebral cavernous malformation2 tests
Cerebroretinal microangiopathy with calcifications and cysts 11 test
Cerebroretinal microangiopathy with calcifications and cysts 21 test
Cernunnos-XLF deficiency1 test
Char syndrome1 test
Charcot-Marie-Tooth disease1 test
Charcot-Marie-Tooth disease, type IA1 test
Chilblain lupus 11 test
Childhood hypophosphatasia1 test
Childhood onset GLUT1 deficiency syndrome 21 test
Childhood-onset cerebral X-linked adrenoleukodystrophy1 test
Chlorpropamide response1 test
Cholangiocarcinoma1 test
Cholestanol storage disease7 tests
Cholestasis, progressive familial intrahepatic, 41 test
Cholestasis, progressive familial intrahepatic, 51 test
Cholesteryl ester storage disease1 test
Chondrodysplasia punctata 2 X-linked dominant1 test
Chromosome 22q11.2 microduplication syndrome1 test
Chronic granulomatous disease1 test
Chronic infantile neurological, cutaneous and articular syndrome1 test
Chylomicron retention disease1 test
Chylomicronemia syndrome1 test
Chédiak-Higashi syndrome3 tests
Citalopram response2 tests
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency1 test
Classic homocystinuria2 tests
Clopidogrel response1 test
Coats plus syndrome1 test
Codeine response1 test
Coenzyme Q10 deficiency1 test
Coenzyme Q10 deficiency, primary, 11 test
Cohen syndrome1 test
Cold-induced sweating syndrome 11 test
Cold-induced sweating syndrome 21 test
Cole-Carpenter syndrome1 test
Colon cancer1 test
Colorectal / endometrial cancer2 tests
Colorectal cancer3 tests
Combined immunodeficiency1 test
Combined immunodeficiency and megaloblastic anemia with or without hyperhomocysteinemia1 test
Combined immunodeficiency due to CD3gamma deficiency3 tests
Combined immunodeficiency due to DOCK8 deficiency3 tests
Combined immunodeficiency due to GINS1 deficiency1 test
Combined immunodeficiency due to LRBA deficiency6 tests
Combined immunodeficiency due to MALT1 deficiency1 test
Combined immunodeficiency due to ORAI1 deficiency2 tests
Combined immunodeficiency due to POLE2 deficiency1 test
Combined immunodeficiency due to STIM1 deficiency4 tests
Combined immunodeficiency due to STK4 deficiency2 tests
Combined immunodeficiency due to partial RAG1 deficiency3 tests
Combined immunodeficiency with faciooculoskeletal anomalies1 test
Combined immunodeficiency, X-linked2 tests
Combined molybdoflavoprotein enzyme deficiency1 test
Combined oxidative phosphorylation defect type 173 tests
Combined oxidative phosphorylation deficiency4 tests
Common variable immunodeficiency3 tests
Complement 3 glomerulopathy1 test
Complement component 2 deficiency1 test
Complement component C1r/C1s deficiency1 test
Complement component C1s deficiency1 test
Complete trisomy 13 syndrome3 tests
Complete trisomy 183 tests
Complex V deficiency1 test
Complex lethal osteochondrodysplasia1 test
Comprehensive testing for inherited renal disease1 test
Congenital adrenal hyperplasia1 test
Congenital cataract-progressive muscular hypotonia-hearing loss-developmental delay syndrome1 test
Congenital chromosomal disease6 tests
Congenital contractural arachnodactyly2 tests
Congenital diarrhea1 test
Congenital diarrhea 5 with tufting enteropathy1 test
Congenital diarrhea 61 test
Congenital diarrhea 7 with exudative enteropathy1 test
Congenital disorder of glycosylation3 tests
Congenital disorder of glycosylation type II1 test
Congenital disorder of glycosylation, type ICC4 tests
Congenital disorder of glycosylation, type IIw2 tests
Congenital dyserythropoietic anemia2 tests
Congenital dyserythropoietic anemia type 41 test
Congenital dyserythropoietic anemia, type I1 test
Congenital dyserythropoietic anemia, type II1 test
Congenital generalized lipodystrophy1 test
Congenital glucose-galactose malabsorption1 test
Congenital heart disease9 tests
Congenital lactase deficiency1 test
Congenital long QT syndrome8 tests
Congenital malabsorptive diarrhea 41 test
Congenital microvillous atrophy1 test
Congenital muscular dystrophy due to LMNA mutation6 tests
Congenital myasthenic syndrome2 tests
Congenital neutropenia2 tests
Congenital neutropenia-myelofibrosis-nephromegaly syndrome1 test
Congenital secretory diarrhea, chloride type1 test
Congenital secretory sodium diarrhea 81 test
Congenital sensory neuropathy with selective loss of small myelinated fibers1 test
Congenital short bowel syndrome, X-linked3 tests
Congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome2 tests
Congenital sodium diarrhea1 test
Conotruncal heart malformations1 test
Corneal intraepithelial dyskeratosis-palmoplantar hyperkeratosis-laryngeal dyskeratosis syndrome1 test
Coronary artery disease, autosomal dominant 22 tests
Costello syndrome5 tests
Cranioectodermal dysplasia 21 test
Creatine transporter deficiency3 tests
Crigler-Najjar syndrome1 test
Crigler-Najjar syndrome type 12 tests
Crigler-Najjar syndrome, type II1 test
Cutaneous porphyria3 tests
Cutis laxa3 tests
Cystic fibrosis2 tests
Cystinuria2 tests
D,L-2-hydroxyglutaric aciduria1 test
D-2-hydroxyglutaric aciduria2 tests
D-2-hydroxyglutaric aciduria 11 test
D-2-hydroxyglutaric aciduria 21 test
DK1-congenital disorder of glycosylation3 tests
DNA ligase IV deficiency2 tests
DOCK2 deficiency1 test
Danon disease4 tests
Deafness-lymphedema-leukemia syndrome3 tests
Deficiency of alpha-mannosidase1 test
Deficiency of guanidinoacetate methyltransferase3 tests
Deficiency of isobutyryl-CoA dehydrogenase3 tests
Deficiency of mevalonate kinase3 tests
Deficiency of ribose-5-phosphate isomerase1 test
Deficiency of steroid 11-beta-monooxygenase1 test
Deficiency of transaldolase1 test
Delayed puberty1 test
Dent disease2 tests
Dent disease type 21 test
Dentatorubral-pallidoluysian atrophy1 test
Desmosterolosis1 test
DiGeorge syndrome2 tests
Diamond-Blackfan anemia 12 tests
Diaphyseal dysplasia2 tests
Diarrhea 10, protein-losing enteropathy type1 test
Diarrhea 12, with microvillus atrophy1 test
Diffuse interstitial pulmonary fibrosis1 test
Dihydropyrimidine dehydrogenase deficiency3 tests
Dilated cardiomyopathy 3B1 test
Disorder of fatty acid metabolism3 tests
Disorder of fatty acid oxidation and ketogenesis1 test
Disorder of galactose metabolism1 test
Disorder of ketone body transport1 test
Disorder of organic acid metabolism1 test
Disorder of phenylalanine metabolism1 test
Disorder of protein N-glycosylation1 test
Disorder of sialic acid metabolism1 test
Disorder of the urea cycle metabolism1 test
Disorder of tyrosine metabolism1 test
Distal renal tubular acidosis1 test
Distal weakness1 test
Dizygotic twins1 test
Dominant beta-thalassemia1 test
Down syndrome3 tests
Drash syndrome1 test
Drug metabolism or response16 tests
Duchenne and Becker muscular dystrophy1 test
Duchenne muscular dystrophy5 tests
Dyskeratosis congenita2 tests
Dyskeratosis congenita, X-linked2 tests
Dyskeratosis congenita, autosomal dominant 11 test
Dyskeratosis congenita, autosomal dominant 21 test
Dyskeratosis congenita, autosomal dominant 31 test
Dyskeratosis congenita, autosomal dominant 41 test
Dyskeratosis congenita, autosomal dominant 61 test
Dyskeratosis congenita, autosomal recessive 11 test
Dyskeratosis congenita, autosomal recessive 21 test
Dyskeratosis congenita, autosomal recessive 31 test
Dyskeratosis congenita, autosomal recessive 52 tests
Dyskeratosis congenita, autosomal recessive 61 test
Dyskeratosis congenita, autosomal recessive 71 test
Dyssynergia1 test
Ectodermal dysplasia1 test
Ectodermal dysplasia and immune deficiency2 tests
Ectodermal dysplasia and immunodeficiency 11 test
Ectodermal dysplasia and immunodeficiency 21 test
Ectodermal dysplasia, X-linked1 test
Ectopia lentis4 tests
Efavirenz response1 test
Ehlers-Danlos syndrome4 tests
Ehlers-Danlos syndrome due to tenascin-X deficiency2 tests
Ehlers-Danlos syndrome, arthrochalasia type3 tests
Ehlers-Danlos syndrome, cardiac valvular type3 tests
Ehlers-Danlos syndrome, classic type4 tests
Ehlers-Danlos syndrome, classic-like, 22 tests
Ehlers-Danlos syndrome, dermatosparaxis type2 tests
Ehlers-Danlos syndrome, musculocontractural type2 tests
Ehlers-Danlos syndrome, periodontal type 21 test
Ehlers-Danlos syndrome, periodontitis type1 test
Ehlers-Danlos syndrome, type 44 tests
Ehlers-Danlos/osteogenesis imperfecta syndrome3 tests
Elliptocytosis 11 test
Elliptocytosis 21 test
Elliptocytosis 31 test
Emery-Dreifuss muscular dystrophy7 tests
Emery-Dreifuss muscular dystrophy 1, X-linked6 tests
Encephalitis, acute, infection (viral)-induced, susceptibility to, 111 test
Encephalomyopathy, mitochondrial, due to voltage-dependent anion channel deficiency1 test
Encephalopathy, acute, infection-induced1 test
Epidermodysplasia verruciformis1 test
Epidermodysplasia verruciformis, susceptibility to, 31 test
Epidermolysis bullosa dystrophica1 test
Epidermolysis bullosa pruriginosa1 test
Epidermolysis bullosa, junctional 7, with interstitial lung disease and nephrotic syndrome1 test
Epilepsy1 test
Episodic pain syndrome, familial, 21 test
Erythrocytosis1 test
Erythropoietic protoporphyria6 tests
Escitalopram response2 tests
Ethylmalonic encephalopathy3 tests
FADD-related immunodeficiency3 tests
Fabry disease14 tests
Facioscapulohumeral muscular dystrophy 4, digenic1 test
Familial Mediterranean fever2 tests
Familial Mediterranean fever, autosomal dominant2 tests
Familial Periodic Fever1 test
Familial amyloid nephropathy with urticaria AND deafness1 test
Familial aortopathy3 tests
Familial apolipoprotein C-II deficiency1 test
Familial cardiomyopathy8 tests
Familial chilblain lupus1 test
Familial chylomicronemia syndrome1 test
Familial cold autoinflammatory syndrome3 tests
Familial cold autoinflammatory syndrome 11 test
Familial cold autoinflammatory syndrome 21 test
Familial cold autoinflammatory syndrome 34 tests
Familial cold autoinflammatory syndrome 41 test
Familial dysautonomia1 test
Familial episodic pain syndrome1 test
Familial episodic pain syndrome with predominantly lower limb involvement1 test
Familial episodic pain syndrome with predominantly upper body involvement1 test
Familial erythrocytosis1 test
Familial hemiplegic migraine1 test
Familial hemophagocytic lymphohistiocytosis3 tests
Familial hemophagocytic lymphohistiocytosis 23 tests
Familial hemophagocytic lymphohistiocytosis 33 tests
Familial hemophagocytic lymphohistiocytosis 43 tests
Familial hemophagocytic lymphohistiocytosis 54 tests
Familial hyperaldosteronism type III1 test
Familial hypercholesterolemia2 tests
Familial hyperkalemic periodic paralysis1 test
Familial hyperreninemic hypoaldosteronism type 21 test
Familial hypobetalipoproteinemia2 tests
Familial hypocalciuric hypercalcemia2 tests
Familial hypocalciuric hypercalcemia 11 test
Familial hypocalciuric hypercalcemia 21 test
Familial hypocalciuric hypercalcemia 31 test
Familial hypokalemia-hypomagnesemia1 test
Familial idiopathic steroid-resistant nephrotic syndrome1 test
Familial intrahepatic cholestasis1 test
Familial isolated dilated cardiomyopathy5 tests
Familial juvenile gout2 tests
Familial pancreatic carcinoma1 test
Familial partial lipodystrophy1 test
Familial prostate cancer1 test
Familial renal hypouricemia1 test
Familial thoracic aortic aneurysm and aortic dissection5 tests
Familial type 3 hyperlipoproteinemia1 test
Fanconi anemia1 test
Fanconi renotubular syndrome 4 with maturity-onset diabetes of the young1 test
Farber lipogranulomatosis1 test
Fatty acyl-CoA reductase 1 deficiency2 tests
Fibrous dysplasia of jaw1 test
Fish-eye disease1 test
Fluoropyrimidine response2 tests
Fluorouracil response2 tests
Fluoxetine response2 tests
Fluvoxamine response2 tests
Focal segmental glomerulosclerosis1 test
Fragile X syndrome1 test
Fragile X-associated tremor/ataxia syndrome1 test
Friedreich ataxia3 tests
Friedreich ataxia 11 test
Friedreich ataxia with retained reflexes1 test
Frontometaphyseal dysplasia3 tests
Frontotemporal dementia and/or amyotrophic lateral sclerosis2 tests
Fucosidosis1 test
Fumarase deficiency1 test
GATA binding protein 1 related thrombocytopenia with dyserythropoiesis1 test
GATA2 deficiency with susceptibility to MDS/AML2 tests
Galactosemia4 tests
Galactosylceramide beta-galactosidase deficiency6 tests
Galloway-Mowat syndrome1 test
Gamma-glutamylcysteine synthetase deficiency2 tests
Gastrointestinal defect and immunodeficiency syndrome1 test
Gaucher disease7 tests
Geleophysic dysplasia4 tests
Generalized pustular psoriasis1 test
Genetic cardiac rhythm disease9 tests
Genetic cerebral small vessel disease1 test
Gilbert syndrome3 tests
Gilbert syndrome, susceptibility to2 tests
Glibenclamide response1 test
Glimepiride response1 test
Glioma1 test
Glipizide response1 test
Global developmental delay1 test
Glomerulopathy with fibronectin deposits 21 test
Glomuvenous malformation1 test
Glucocorticoid-remediable aldosteronism1 test
Glucose-6-phosphate transport defect3 tests
Glutaric acidemia IIa1 test
Glutaric acidemia IIb1 test
Glutaric acidemia IIc1 test
Glutaric aciduria, type 13 tests
Glutathione synthetase deficiency without 5-oxoprolinuria2 tests
Glycogen storage disease8 tests
Glycogen storage disease IIIa3 tests
Glycogen storage disease IIIb3 tests
Glycogen storage disease due to glucose-6-phosphatase deficiency type IA1 test
Glycogen storage disease due to phosphoglycerate kinase 1 deficiency1 test
Glycogen storage disease, type I2 tests
Glycogen storage disease, type II11 tests
Glycogen storage disease, type VII2 tests
Gnathodiaphyseal dysplasia1 test
Granulomatous disease, chronic, X-linked1 test
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 21 test
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 31 test
Griscelli syndrome type 22 tests
Growth hormone insensitivity syndrome with immune dysregulation 2, autosomal dominant2 tests
Growth hormone insensitivity with immune dysregulation 1, autosomal recessive2 tests
HNSHA due to aldolase A deficiency2 tests
Hashimoto thyroiditis1 test
Hearing loss, autosomal dominant 34, with or without inflammation1 test
Hematologic disorder1 test
Hematologic neoplasm2 tests
Heme oxygenase 1 deficiency2 tests
Hemolytic anemia2 tests
Hemolytic anemia due to adenylate kinase deficiency2 tests
Hemolytic anemia due to glucophosphate isomerase deficiency2 tests
Hemolytic anemia due to glutathione reductase deficiency1 test
Hemolytic anemia due to hexokinase deficiency2 tests
Hemolytic anemia due to pyrimidine 5' nucleotidase deficiency2 tests
Hepatic methionine adenosyltransferase deficiency1 test
Hepatitis B virus, susceptibility to2 tests
Hepatitis C virus infection, response to therapy of1 test
Hepatoerythropoietic porphyria2 tests
Hereditary Paraganglioma-Pheochromacytoma Syndrome1 test
Hereditary Wilms tumor1 test
Hereditary acrodermatitis enteropathica1 test
Hereditary acrokeratotic poikiloderma, Weary type1 test
Hereditary breast and/or gynecological cancer syndrome1 test
Hereditary breast ovarian cancer syndrome1 test
Hereditary cancer-predisposing syndrome3 tests
Hereditary coproporphyria6 tests
Hereditary diffuse gastric adenocarcinoma1 test
Hereditary disease5 tests
Hereditary elliptocytosis1 test
Hereditary endocrine tumor syndrome1 test
Hereditary factor IX deficiency disease1 test
Hereditary gastrointestinal cancer and/or polyposis syndrome1 test
Hereditary hearing loss and deafness1 test
Hereditary hemochromatosis1 test
Hereditary hemorrhagic telangiectasia2 tests
Hereditary hyperbilirubinemia1 test
Hereditary insensitivity to pain with anhidrosis1 test
Hereditary leiomyomatosis and renal cell cancer1 test
Hereditary liability to pressure palsies1 test
Hereditary lipodystrophy1 test
Hereditary motor and sensory neuropathy1 test
Hereditary neutrophilia1 test
Hereditary non-spherocytic hemolytic anemia2 tests
Hereditary pancreatitis2 tests
Hereditary sensory and autonomic neuropathy type 61 test
Hereditary sensory and autonomic neuropathy type 71 test
Hereditary sensory and autonomic neuropathy with spastic paraplegia1 test
Hereditary sensory neuropathy-deafness-dementia syndrome1 test
Hereditary spastic paraplegia1 test
Hereditary spherocytosis1 test
Hereditary spherocytosis type 11 test
Hereditary spherocytosis type 21 test
Hereditary spherocytosis type 31 test
Hereditary spherocytosis type 41 test
Hereditary spherocytosis type 51 test
Hereditary stomatocytosis1 test
Hereditary xanthinuria1 test
Hereditary xanthinuria type 11 test
Heritable Thoracic Aortic Disease3 tests
Hermansky-Pudlak syndrome3 tests
Hermansky-Pudlak syndrome 11 test
Hermansky-Pudlak syndrome 103 tests
Hermansky-Pudlak syndrome 23 tests
Hermansky-Pudlak syndrome 31 test
Hermansky-Pudlak syndrome 41 test
Hermansky-Pudlak syndrome 61 test
Hermansky-Pudlak syndrome 91 test
Herpes simplex encephalitis1 test
Holt-Oram syndrome1 test
Homocystinuria3 tests
Hormone receptor-positive breast cancer2 tests
Huntington disease1 test
Hutchinson-Gilford syndrome1 test
Hyper-IgE recurrent infection syndrome 1, autosomal dominant5 tests
Hyper-IgE recurrent infection syndrome 3, autosomal recessive2 tests
Hyper-IgE recurrent infection syndrome 4, autosomal recessive1 test
Hyper-IgE recurrent infection syndrome 4A, autosomal dominant1 test
Hyper-IgE recurrent infection syndrome 5, autosomal recessive1 test
Hyper-IgE syndrome2 tests
Hyper-IgM syndrome type 12 tests
Hyper-IgM syndrome type 21 test
Hypercalcemia, infantile, 11 test
Hypercalcemia, infantile, 21 test
Hypercalciuria, absorptive, 11 test
Hyperimmunoglobulin D with periodic fever3 tests
Hyperimmunoglobulin M syndrome2 tests
Hyperlipidemia due to hepatic triglyceride lipase deficiency1 test
Hyperlipidemia, familial combined, LPL related2 tests
Hyperlipoproteinemia2 tests
Hyperlipoproteinemia, type 1D1 test
Hyperlipoproteinemia, type I2 tests
Hyperoxaluria1 test
Hypertriglyceridemia 11 test
Hypertrophic cardiomyopathy6 tests
Hyperuricemic nephropathy, familial juvenile type 41 test
Hypobetalipoproteinemia1 test
Hypogonadotropic hypogonadism 5 with or without anosmia1 test
Hypokalemic periodic paralysis1 test
Hypomagnesemia, seizures, and intellectual disability1 test
Hypoparathyroidism1 test
Hypoparathyroidism, deafness, renal disease syndrome1 test
Hypophosphatasia2 tests
Hypophosphatemic nephrolithiasis/osteoporosis 11 test
Hypophosphatemic nephrolithiasis/osteoporosis 21 test
Hypophosphatemic rickets1 test
Hypouricemia, renal, 21 test
Hypoxanthine-guanine phosphoribosyltransferase deficiency1 test
IKBKG-related immunodeficiency with or without ectodermal dysplasia3 tests
IL21-related infantile inflammatory bowel disease2 tests
IMAGe syndrome1 test
Ichthyosis linearis circumflexa1 test
Imerslund-Grasbeck syndrome type 11 test
Immune dysregulation disease with immunodeficiency2 tests
Immunodeficiency 1042 tests
Immunodeficiency 106, susceptibility to viral infections1 test
Immunodeficiency 109 with lymphoproliferation3 tests
Immunodeficiency 115 with autoinflammation1 test
Immunodeficiency 11b with atopic dermatitis6 tests
Immunodeficiency 145 tests
Immunodeficiency 14b, autosomal recessive5 tests
Immunodeficiency 181 test
Immunodeficiency 191 test
Immunodeficiency 231 test
Immunodeficiency 251 test
Immunodeficiency 31B4 tests
Immunodeficiency 31C, autosomal dominant2 tests
Immunodeficiency 332 tests
Immunodeficiency 351 test
Immunodeficiency 364 tests
Immunodeficiency 391 test
Immunodeficiency 452 tests
Immunodeficiency 471 test
Immunodeficiency 491 test
Immunodeficiency 511 test
Immunodeficiency 573 tests
Immunodeficiency 602 tests
Immunodeficiency 611 test
Immunodeficiency 63 with lymphoproliferation and autoimmunity4 tests
Immunodeficiency 643 tests
Immunodeficiency 65, susceptibility to viral infections1 test
Immunodeficiency 73b with defective neutrophil chemotaxis and lymphopenia3 tests
Immunodeficiency 73c with defective neutrophil chemotaxis and hypogammaglobulinemia3 tests
Immunodeficiency 74, COVID-19-related, X-linked2 tests
Immunodeficiency 753 tests
Immunodeficiency 761 test
Immunodeficiency 78 with autoimmunity and developmental delay3 tests
Immunodeficiency 811 test
Immunodeficiency 83, susceptibility to viral infections1 test
Immunodeficiency 87 and autoimmunity4 tests
Immunodeficiency 94 with autoinflammation and dysmorphic facies1 test
Immunodeficiency 951 test
Immunodeficiency 961 test
Immunodeficiency 98 with autoinflammation, X-linked1 test
Immunodeficiency due to CD25 deficiency3 tests
Immunodeficiency due to defect in CD3-gamma1 test
Immunodeficiency, Polyendocrinopathy, and Enteropathy X-Linked Syndrome1 test
Immunodeficiency, X-linked, with hyper-IgM1 test
Immunodeficiency, common variable, 13 tests
Immunodeficiency, common variable, 101 test
Immunodeficiency, common variable, 121 test
Immunodeficiency, common variable, 141 test
Immunodeficiency, common variable, 21 test
Immunodeficiency, common variable, 31 test
Immunodeficiency, common variable, 41 test
Immunodeficiency, common variable, 51 test
Immunodeficiency, common variable, 61 test
Immunodeficiency, common variable, 71 test
Immunodeficiency, common variable, due to APRIL deficiency1 test
Immunodeficiency-centromeric instability-facial anomalies syndrome 11 test
Immunodeficiency-centromeric instability-facial anomalies syndrome 21 test
Immunodeficiency-centromeric instability-facial anomalies syndrome 31 test
Immunoglobulin A deficiency 21 test
Immunoskeletal dysplasia with neurodevelopmental abnormalities1 test
Inborn disorder of bile acid synthesis1 test
Inborn disorder of cobalamin metabolism and transport1 test
Inborn disorder of purine or pyrimidine metabolism2 tests
Inborn errors of metabolism2 tests
Inborn mitochondrial myopathy1 test
Incontinentia pigmenti syndrome3 tests
Increased HDL cholesterol concentration1 test
Infantile Krabbe disease5 tests
Infantile hypophosphatasia1 test
Infantile-onset periodic fever-panniculitis-dermatosis syndrome1 test
Infertility disorder1 test
Inflammatory bowel disease2 tests
Inflammatory bowel disease 253 tests
Inflammatory bowel disease 283 tests
Inflammatory bowel disease, immunodeficiency, and encephalopathy2 tests
Inflammatory skin and bowel disease, neonatal, 12 tests
Inherited renal cancer-predisposing syndrome1 test
Inherited rippling muscle disease2 tests
Insulin-dependent diabetes mellitus secretory diarrhea syndrome1 test
Intestinal hypomagnesemia 11 test
Intestinal pseudoobstruction, neuronal, chronic idiopathic, X-linked3 tests
Irinotecan response2 tests
Jervell and Lange-Nielsen syndrome4 tests
Joubert syndrome 101 test
Junctional epidermolysis bullosa1 test
Juvenile arthritis due to defect in LACC11 test
Juvenile myelomonocytic leukemia1 test
Juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome4 tests
Kabuki syndrome 11 test
Kabuki syndrome 21 test
Karyomegalic interstitial nephritis1 test
Kearns-Sayre syndrome1 test
Kennedy disease1 test
Keppen-Lubinsky syndrome1 test
Keratitis fugax hereditaria1 test
Keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome1 test
Ketamine response1 test
Kidney disorder1 test
Kindler syndrome1 test
Klinefelter syndrome2 tests
Kostmann syndrome1 test
Kyphoscoliotic Ehlers-Danlos syndrome2 tests
L-2-hydroxyglutaric aciduria2 tests
LIPE-related familial partial lipodystrophy1 test
LRP5-related primary osteoporosis1 test
Larsen-like syndrome, B3GAT3 type2 tests
Late-infantile/juvenile Krabbe disease1 test
Lateral meningocele syndrome1 test
Lathosterolosis1 test
Lazy leukocyte syndrome1 test
Left ventricular noncompaction6 tests
Left ventricular noncompaction cardiomyopathy6 tests
Legius syndrome1 test
Leigh Syndrome (mtDNA mutation)1 test
Leigh Syndrome (nuclear DNA mutation)1 test
Leigh syndrome2 tests
Leigh syndrome due to mitochondrial complex IV deficiency1 test
Leigh syndrome due to mitochondrial complex V deficiency1 test
Lesch-Nyhan syndrome2 tests
Leukemia, acute myeloid, susceptibility to1 test
Leukocyte adhesion deficiency2 tests
Leukocyte adhesion deficiency 11 test
Liddle syndrome 11 test
Liddle syndrome 21 test
Limb-girdle muscular dystrophy5 tests
Lipase deficiency, combined1 test
Lipodystrophy1 test
Lipogranulomatosis1 test
Loeys-Dietz syndrome4 tests
Loeys-Dietz syndrome 12 tests
Loeys-Dietz syndrome 22 tests
Long QT syndrome8 tests
Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency1 test
Lowe syndrome2 tests
Lung cancer1 test
Lymphoma, non-Hodgkin, familial1 test
Lymphoproliferative syndrome 13 tests
Lymphoproliferative syndrome 24 tests
Lynch syndrome2 tests
Lynch syndrome 81 test
Lysinuric protein intolerance1 test
Lysosomal acid lipase deficiency2 tests
Lysosomal storage disease3 tests
MASS syndrome4 tests
MELAS syndrome1 test
MEND syndrome1 test
MHC class II deficiency 21 test
MHC class II deficiency 31 test
MHC class II deficiency 41 test
MHC class II deficiency 51 test
MOGS-congenital disorder of glycosylation1 test
MPI-congenital disorder of glycosylation1 test
MYO5B-related progressive familial intrahepatic cholestasis1 test
Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss1 test
Macrothrombocytopenia-lymphedema-developmental delay-facial dysmorphism-camptodactyly syndrome2 tests
Majeed syndrome1 test
Malignant hematological disorder1 test
Mandibuloacral dysplasia with type B lipodystrophy2 tests
Maple syrup urine disease1 test
Marfan syndrome4 tests
McLeod neuroacanthocytosis syndrome1 test
Meconium ileus1 test
Medium-chain acyl-coenzyme A dehydrogenase deficiency2 tests
Meester-Loeys syndrome2 tests
Melanoma1 test
Melnick-Needles syndrome3 tests
Mendelian susceptibility to mycobacterial diseases due to complete ISG15 deficiency1 test
Mendelian susceptibility to mycobacterial diseases due to partial STAT1 deficiency4 tests
Menkes kinky-hair syndrome2 tests
Mercaptopurine response1 test
Metabolic myopathy1 test
Metachondromatosis1 test
Metachromatic leukodystrophy2 tests
Metaphyseal chondrodysplasia, McKusick type1 test
Metaphyseal dysplasia without hypotrichosis1 test
Methadone response1 test
Methylmalonic acidemia4 tests
Methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency1 test
Mevalonic aciduria3 tests
Migraine1 test
Miscarriage1 test
Mitochondrial DNA Deletion Syndromes1 test
Mitochondrial complex 4 deficiency, nuclear type 111 test
Mitochondrial complex I deficiency5 tests
Mitochondrial complex I deficiency, mitochondrial type1 test
Mitochondrial complex II deficiency, nuclear type 11 test
Mitochondrial complex III deficiency1 test
Mitochondrial complex V (ATP synthase) deficiency nuclear type 24 tests
Mitochondrial disease5 tests
Mitochondrial disorder due to a defect in mitochondrial protein synthesis1 test
Mitochondrial encephalomyopathy1 test
Mitochondrial encephalopathy1 test
Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency3 tests
Mitochondrial myopathy with diabetes1 test
Mitochondrial myopathy, episodic, with optic atrophy and reversible leukoencephalopathy1 test
Mitochondrial myopathy, isolated1 test
Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome1 test
Mitochondrial neurogastrointestinal encephalomyopathy1 test
Mitochondrial oxidative phosphorylation disorder1 test
Mitochondrial oxidative phosphorylation disorder due to a large-scale single deletion of mitochondrial DNA1 test
Mitochondrial oxidative phosphorylation disorder due to a point mutation of mitochondrial DNA1 test
Mitochondrial oxidative phosphorylation disorder due to mitochondrial DNA anomalies1 test
Mitochondrial trifunctional protein deficiency1 test
Monocytopenia with susceptibility to infections3 tests
Monosomy 7 myelodysplasia and leukemia syndrome 11 test
Motor neuron disease1 test
Moyamoya disease3 tests
Mucolipidosis type II1 test
Mucopolysaccharidoses, unclassified types1 test
Mucopolysaccharidosis4 tests
Mucopolysaccharidosis type 14 tests
Mucopolysaccharidosis type 64 tests
Mucopolysaccharidosis type 74 tests
Mucopolysaccharidosis, MPS-II6 tests
Mucopolysaccharidosis, MPS-III-A4 tests
Mucopolysaccharidosis, MPS-III-B4 tests
Mucopolysaccharidosis, MPS-III-C4 tests
Mucopolysaccharidosis, MPS-III-D2 tests
Mucopolysaccharidosis, MPS-IV-A4 tests
Mucopolysaccharidosis, MPS-IV-B4 tests
Multiple acyl-CoA dehydrogenase deficiency4 tests
Multiple cutaneous and mucosal venous malformations2 tests
Multiple endocrine neoplasia, type 21 test
Multiple gastrointestinal atresias1 test
Multiple self-healing squamous epithelioma2 tests
Multiple sulfatase deficiency5 tests
Muscular dystrophy1 test
Muscular dystrophy-dystroglycanopathy3 tests
Myelodysplastic syndrome2 tests
Myofibrillar myopathy6 tests
Myopathy with giant abnormal mitochondria1 test
Myopathy, lactic acidosis, and sideroblastic anemia1 test
Myopathy, tubular aggregate, 14 tests
Myopathy, tubular aggregate, 21 test
Myosin storage myopathy3 tests
NARP syndrome2 tests
Nail-patella syndrome1 test
Naxos disease5 tests
Nemaline myopathy3 tests
Neonatal Marfan syndrome4 tests
Neonatal severe primary hyperparathyroidism2 tests
Nephrogenic diabetes insipidus1 test
Nephrogenic syndrome of inappropriate antidiuresis1 test
Nephrolithiasis/nephrocalcinosis1 test
Nephronophthisis1 test
Nephrotic syndrome1 test
Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures1 test
Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion1 test
Neurohypophyseal diabetes insipidus1 test
Neuromuscular disease1 test
Neuronal ceroid lipofuscinosis2 tests
Neuronal ceroid lipofuscinosis 12 tests
Neuronal ceroid lipofuscinosis 22 tests
Neuronopathy, distal hereditary motor, type 2A1 test
Neuronopathy, distal hereditary motor, type 2B1 test
Neuronopathy, distal hereditary motor, type 2D1 test
Neuronopathy, distal hereditary motor, type 5A1 test
Neuronopathy, distal hereditary motor, type 5C1 test
Neuronopathy, distal hereditary motor, type 7A1 test
Neuronopathy, distal hereditary motor, type 7B1 test
Neuropathy, hereditary sensory and autonomic, type 1A1 test
Neuropathy, hereditary sensory and autonomic, type 1C1 test
Neuropathy, hereditary sensory and autonomic, type 2A1 test
Neuropathy, hereditary sensory and autonomic, type 2B1 test
Neuropathy, hereditary sensory and autonomic, type IId1 test
Neuropathy, hereditary sensory, type 1D1 test
Neuropathy, hereditary sensory, type 1F1 test
Neuropathy, hereditary sensory, type 2C1 test
Neutropenia, severe congenital, 1, autosomal dominant1 test
Neutropenia, severe congenital, 2, autosomal dominant1 test
Neutropenia, severe congenital, 8, autosomal dominant1 test
Neutropenia, severe congenital, 9, autosomal dominant1 test
Neutrophil immunodeficiency syndrome3 tests
Nevirapine response1 test
Nicotine dependence1 test
Niemann-Pick disease, type A7 tests
Niemann-Pick disease, type B7 tests
Niemann-Pick disease, type C3 tests
Nijmegen breakage syndrome-like disorder1 test
Nilotinib response2 tests
Non-small cell lung carcinoma1 test
Nonimmune chronic idiopathic neutropenia of adults1 test
Nonsteroidal anti-inflammatory drug response1 test
Nonsyndromic congenital nail disorder 81 test
Noonan syndrome6 tests
Noonan syndrome and Noonan-related syndrome5 tests
Noonan syndrome with multiple lentigines5 tests
Noonan syndrome-like disorder with loose anagen hair6 tests
Noonan-like syndrome1 test
Norum disease1 test
Obesity due to prohormone convertase I deficiency1 test
Odontohypophosphatasia1 test
Oligosaccharidosis1 test
Ondansetron response1 test
Ophthalmoplegic neuromuscular disorder with abnormal mitochondria1 test
Orofaciodigital syndrome I2 tests
Osteogenesis imperfecta3 tests
Osteogenesis imperfecta type 101 test
Osteogenesis imperfecta type 111 test
Osteogenesis imperfecta type 121 test
Osteogenesis imperfecta type 131 test
Osteogenesis imperfecta type 141 test
Osteogenesis imperfecta type 151 test
Osteogenesis imperfecta type 161 test
Osteogenesis imperfecta type 173 tests
Osteogenesis imperfecta type 51 test
Osteogenesis imperfecta type 61 test
Osteogenesis imperfecta type 71 test
Osteogenesis imperfecta type 81 test
Osteogenesis imperfecta type 91 test
Osteogenesis imperfecta type I1 test
Osteogenesis imperfecta type III1 test
Osteogenesis imperfecta, CREB3L1 related1 test
Osteogenesis imperfecta, type III/IV1 test
Osteootohepatoenteric syndrome1 test
Osteopetrosis with renal tubular acidosis1 test
Otofaciocervical syndrome 22 tests
Otopalatodigital Spectrum Disorders3 tests
PLIN1-related familial partial lipodystrophy1 test
PMM2-congenital disorder of glycosylation4 tests
POLR3-related leukodystrophy1 test
PPARG-related familial partial lipodystrophy1 test
PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 3, DIGENIC1 test
PTEN hamartoma tumor syndrome1 test
Pancreatic adenocarcinoma1 test
Pancytopenia due to IKZF1 mutations2 tests
Parkinson disease1 test
Paroxetine response2 tests
Partial adenosine deaminase deficiency4 tests
Partial hypoxanthine-guanine phosphoribosyltransferase deficiency1 test
Pazopanib response3 tests
Pearson syndrome1 test
Peginterferon alfa-2a response1 test
Peginterferon alfa-2b response1 test
Pegloticase response1 test
Pelger-Huet-like anomaly and episodic fever with abdominal pain1 test
Periodic fever-infantile enterocolitis-autoinflammatory syndrome2 tests
Peripheral neuropathy2 tests
Periventricular nodular heterotopia3 tests
Peroxisome biogenesis disorder6 tests
Peroxisome biogenesis disorder 1A (Zellweger)1 test
Peutz-Jeghers syndrome1 test
Phenylketonuria1 test
Phenytoin response2 tests
Phenytoin toxicity2 tests
Phosphate transport defect1 test
Phosphoenolpyruvate carboxykinase deficiency, mitochondrial1 test
Phosphoribosylpyrophosphate synthetase superactivity1 test
Pityriasis rubra pilaris1 test
Platelet abnormalities with eosinophilia and immune-mediated inflammatory disease2 tests
Poikiloderma with neutropenia2 tests
Polycystic kidney disease1 test
Polycystic liver disease 4 with or without kidney cysts1 test
Polyendocrinopathy1 test
Polyglandular autoimmune syndrome, type 12 tests
Polyglucosan body myopathy1 test
Polyglucosan body myopathy 1 with immunodeficiency1 test
Polyglucosan body myopathy 1 without immunodeficiency1 test
Polyglucosan body myopathy type 11 test
Porokeratosis1 test
Porokeratosis 3, disseminated superficial actinic type2 tests
Porphobilinogen synthase deficiency3 tests
Porphyria3 tests
Porphyria cutanea tarda5 tests
Prader-Willi syndrome1 test
Prader-Willi syndrome due to maternal uniparental disomy of chromosome 151 test
Predisposition to invasive fungal disease due to CARD9 deficiency1 test
Premature ovarian failure1 test
Premature ovarian failure 11 test
Primary CD59 deficiency1 test
Primary ciliary dyskinesia1 test
Primary dilated cardiomyopathy7 tests
Primary familial dilated cardiomyopathy7 tests
Primary familial hypertrophic cardiomyopathy6 tests
Primary hyperoxaluria2 tests
Primary hyperoxaluria type 32 tests
Primary hyperoxaluria, type I2 tests
Primary hyperoxaluria, type II2 tests
Primary immunodeficiency with predisposition to severe viral infection1 test
Progeroid and marfanoid aspect-lipodystrophy syndrome4 tests
Progressive external ophthalmoplegia1 test
Progressive familial intrahepatic cholestasis1 test
Progressive familial intrahepatic cholestasis type 31 test
Prolidase deficiency1 test
Propionic acidemia6 tests
Proteasome-associated autoinflammatory syndrome 11 test
Proteasome-associated autoinflammatory syndrome 21 test
Proteasome-associated autoinflammatory syndrome 31 test
Proteasome-associated autoinflammatory syndrome 41 test
Proteasome-associated autoinflammatory syndrome 51 test
Protein-losing enteropathy2 tests
Proteinuria, low molecular weight, with hypercalciuria and nephrocalcinosis1 test
Proton pump inhibitor response1 test
Proximal renal tubular acidosis1 test
Pseudo-TORCH syndrome1 test
Pseudo-TORCH syndrome 21 test
Pseudo-TORCH syndrome 32 tests
Pseudohypoaldosteronism type 11 test
Pseudohypoaldosteronism type 2B1 test
Pseudohypoaldosteronism type 2C1 test
Pseudohypoaldosteronism type 2D1 test
Pseudohypoaldosteronism type 2E1 test
Pseudoxanthoma elasticum1 test
Psoriasis 13, susceptibility to1 test
Psoriasis 21 test
Pulmonary alveolar proteinosis with hypogammaglobulinemia1 test
Pulmonary fibrosis and/or bone marrow failure, Telomere-related, 11 test
Pulmonary fibrosis and/or bone marrow failure, Telomere-related, 32 tests
Pulmonary fibrosis and/or bone marrow failure, Telomere-related, 41 test
Pulmonary fibrosis and/or bone marrow failure, telomere-related, 51 test
Pulmonary fibrosis and/or bone marrow failure, telomere-related, 61 test
Pulmonary fibrosis, idiopathic, susceptibility to1 test
Pulmonary hypertension, familial primary, 1, with or without HHT1 test
Pure gonadal dysgenesis 46,XY1 test
Pure mitochondrial myopathy1 test
Purine-nucleoside phosphorylase deficiency1 test
Pyogenic arthritis-pyoderma gangrenosum-acne syndrome1 test
Pyropoikilocytosis, hereditary1 test
Pyruvate kinase deficiency of red cells3 tests
Qualitative or quantitative defects of dystrophin1 test
RASopathy6 tests
RIDDLE syndrome1 test
Rasburicase response1 test
Recombinase activating gene 2 deficiency2 tests
Reducing body myopathy3 tests
Renal carnitine transport defect4 tests
Renal cysts and diabetes syndrome1 test
Renal hypomagnesemia 21 test
Renal hypomagnesemia 41 test
Renal hypomagnesemia 5 with ocular involvement1 test
Renal hypomagnesemia 61 test
Renal tubular acidosis with progressive nerve deafness1 test
Renal-hepatic-pancreatic dysplasia1 test
Reticular dysgenesis2 tests
Retinal dystrophy and microvillus inclusion disease1 test
Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations2 tests
Retinitis pigmentosa and erythrocytic microcytosis3 tests
Revesz syndrome1 test
Rh-null, regulator type1 test
Rhabdomyolysis1 test
Rhizomelic chondrodysplasia punctata3 tests
Ribavirin response1 test
Rippling muscle disease2 tests
Rosuvastatin response1 test
Russell-Silver syndrome1 test
SCID due to ADA deficiency, delayed onset1 test
SHORT syndrome5 tests
STAT3-related early-onset multisystem autoimmune disease4 tests
STING-associated vasculopathy with onset in infancy1 test
Sandhoff disease1 test
Schimke immuno-osseous dysplasia2 tests
Selective serotonin reuptake inhibitor response2 tests
Sertraline response2 tests
Severe combined immunodeficiency disease4 tests
Severe combined immunodeficiency due to CARD11 deficiency7 tests
Severe combined immunodeficiency due to CARMIL2 deficiency4 tests
Severe combined immunodeficiency due to CD70 deficiency4 tests
Severe combined immunodeficiency due to CORO1A deficiency3 tests
Severe combined immunodeficiency due to CTPS1 deficiency3 tests
Severe combined immunodeficiency due to DCLRE1C deficiency1 test
Severe combined immunodeficiency due to LAT deficiency1 test
Severe combined immunodeficiency, B cell-negative1 test
Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency3 tests
Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-positive2 tests
Severe congenital neutropenia4 tests
Sex-linked hereditary disorder3 tests
Short QT syndrome5 tests
Shprintzen-Goldberg syndrome2 tests
Shwachman syndrome1 test
Shwachman-Diamond syndrome 11 test
Shwachman-Diamond syndrome 21 test
Sick sinus syndrome6 tests
Silver-Russell syndrome 11 test
Silver-Russell syndrome due to maternal uniparental disomy of chromosome 71 test
Simpson-Golabi-Behmel syndrome type 21 test
Simvastatin response1 test
Singleton-Merten syndrome 13 tests
Singleton-Merten syndrome 21 test
Sinus histiocytosis with massive lymphadenopathy1 test
Sitosterolemia2 tests
Smith-Lemli-Opitz syndrome2 tests
Sneddon syndrome4 tests
Solid tumor3 tests
Southeast Asian ovalocytosis1 test
Spastic paraplegia1 test
Specific granule deficiency 11 test
Specific granule deficiency 21 test
Sphingolipid activator protein 1 deficiency1 test
Spinal muscular atrophy3 tests
Spinal muscular atrophy-progressive myoclonic epilepsy syndrome2 tests
Spinocerebellar ataxia 491 test
Spinocerebellar ataxia 71 test
Spinocerebellar ataxia type 11 test
Spinocerebellar ataxia type 21 test
Spinocerebellar ataxia type 61 test
Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 21 test
Spondylo-ocular syndrome1 test
Spondylodysplastic Ehlers-Danlos syndrome2 tests
Spondyloenchondrodysplasia with immune dysregulation1 test
Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures2 tests
Stage IV Non-Small Cell Lung Cancer1 test
Statin causing adverse effect in therapeutic use1 test
Statin-induced myopathy1 test
Sterile multifocal osteomyelitis with periostitis and pustulosis1 test
Stiff skin syndrome4 tests
Stormorken syndrome4 tests
Stuve-Wiedemann syndrome 21 test
Subcutaneous panniculitis-like T-cell lymphoma1 test
Sucrase-isomaltase deficiency1 test
Sudden unexplained death1 test
Sulfite oxidase deficiency1 test
Supravalvar aortic stenosis1 test
Susceptibility to HIV infection2 tests
Susceptibility to respiratory infections associated with CD8alpha chain mutation1 test
Symmetrical dyschromatosis of extremities1 test
Syndrome of entercolitis and autoinflmmation caused by mutation of NLRC4 (SCAN4)1 test
Syndromic congenital sodium diarrhea1 test
Syndromic intellectual disability1 test
Syndromic multisystem autoimmune disease due to ITCH deficiency3 tests
Systemic lupus erythematosus 172 tests
Systemic lupus erythematosus, susceptibility to, 11 test
T-cell immunodeficiency, congenital alopecia, and nail dystrophy1 test
T-cell lymphopenia, infantile, with or without nail dystrophy, autosomal dominant1 test
TNF receptor-associated periodic fever syndrome (TRAPS)1 test
Tacrolimus response1 test
Tafenoquine response1 test
Tamoxifen response1 test
Tay-Sachs disease1 test
Telomere syndrome1 test
Terminal osseous dysplasia-pigmentary defects syndrome3 tests
Tetralogy of Fallot1 test
Tetraploidy syndrome2 tests
Thioguanine response1 test
Thiopurine S-methyltransferase deficiency1 test
Thiopurine metabolic disease1 test
Thiopurine response1 test
Thiopurines, poor metabolism of, 21 test
Thrombocytopenia 12 tests
Thrombocytopenia, X-linked, intermittent2 tests
Thrombophilia1 test
Thrombotic microangiopathy1 test
Thyroid dyshormonogenesis 61 test
Thyroid gland carcinoma1 test
Tibial muscular dystrophy5 tests
Tolbutamide response1 test
Transient bullous dermolysis of the newborn1 test
Transient infantile hypertriglyceridemia and hepatosteatosis1 test
Trichohepatoenteric syndrome2 tests
Trichohepatoenteric syndrome 11 test
Trichohepatoenteric syndrome 22 tests
Tricyclic antidepressant response2 tests
Triosephosphate isomerase deficiency2 tests
Triploidy2 tests
Trisomy2 tests
Trisomy X syndrome1 test
Tropisetron response1 test
Tuberous sclerosis 11 test
Tuberous sclerosis 21 test
Tuberous sclerosis syndrome2 tests
Tumoral calcinosis, hyperphosphatemic, familial, 11 test
Tumoral calcinosis, hyperphosphatemic, familial, 21 test
Tumoral calcinosis, hyperphosphatemic, familial, 31 test
Turner syndrome5 tests
Twinning, monozygotic1 test
Tyrosinemia1 test
Tyrosinemia type I1 test
Uniparental disomy of maternal origin1 test
Uniparental disomy of paternal origin1 test
Upshaw-Schulman syndrome1 test
VACTERL association1 test
Varicella, severe recurrent1 test
Variegate porphyria6 tests
Vasculitis due to ADA2 deficiency4 tests
Velocardiofacial syndrome1 test
Ventricular arrhythmias due to cardiac ryanodine receptor calcium release deficiency syndrome6 tests
Ventricular fibrillation6 tests
Ventriculomegaly-cystic kidney disease2 tests
Very long chain acyl-CoA dehydrogenase deficiency6 tests
Vitamin B12-responsive methylmalonic acidemia1 test
Vitamin D hydroxylation-deficient rickets, type 1B1 test
Vitamin D-dependent rickets, type 11 test
Von Hippel-Lindau syndrome2 tests
Voriconazole response1 test
WHIM syndrome 11 test
WHIM syndrome 21 test
Warfarin response2 tests
Warts, hypogammaglobulinemia, infections, and myelokathexis2 tests
Weill-Marchesani syndrome3 tests
Wiedemann-Steiner syndrome1 test
Wilms tumor 11 test
Wilson disease2 tests
Wiskott-Aldrich syndrome5 tests
Wiskott-Aldrich syndrome 23 tests
Wolff-Parkinson-White pattern5 tests
Wolman disease2 tests
X-linked Alport syndrome1 test
X-linked Mendelian susceptibility to mycobacterial diseases due to CYBB deficiency1 test
X-linked agammaglobulinemia3 tests
X-linked agammaglobulinemia with growth hormone deficiency1 test
X-linked cerebral adrenoleukodystrophy3 tests
X-linked distal spinal muscular atrophy type 32 tests
X-linked erythropoietic protoporphyria5 tests
X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection and neoplasia2 tests
X-linked intellectual disability with marfanoid habitus2 tests
X-linked intellectual disability, van Esch type2 tests
X-linked lymphoproliferative disease due to SH2D1A deficiency7 tests
X-linked lymphoproliferative disease due to XIAP deficiency7 tests
X-linked lymphoproliferative syndrome6 tests
X-linked myopathy with postural muscle atrophy3 tests
X-linked osteoporosis with fractures1 test
X-linked reticulate pigmentary disorder2 tests
X-linked severe combined immunodeficiency1 test
X-linked severe congenital neutropenia5 tests
X-linked spondyloepimetaphyseal dysplasia2 tests
Xanthinuria type II1 test
Xerocytosis1 test
ZAP70-Related Severe Combined Immunodeficiency3 tests
Zellweger spectrum disorders4 tests
delta Thalassemia2 tests
methadone response - Dosage1 test