U.S. flag

An official website of the United States government

Athena Diagnostics

General information

Athena Diagnostics

200 Forest Street
2nd Floor
Marlborough
Massachusetts
United States - 01752
http://www.athenadiagnostics.com/
Organization ID: 1012

Personnel

View this laboratory in GTR

Assertion criteria

Level: Assertion criteria provided

Summary of submissions to ClinVar

Total submissions: 19757

Gene

GeneSubmissionsLast Updated
ABAT14Dec 30, 2020
ABCA31Dec 30, 2022
ABCC892Jan 3, 2024
ABCD132Jan 3, 2024
ABHD124Sep 25, 2019
ACAD92Dec 30, 2022
ACTA12Jan 3, 2024
ACTB5Oct 2, 2024
ACTC11Dec 30, 2022
ACTG113Sep 13, 2021
ACTN422Dec 30, 2020
ADA1Dec 30, 2022
ADCY16Sep 25, 2019
ADGRG123Dec 27, 2022
ADGRV1126Jan 3, 2024
ADNP1Dec 30, 2022
ADSL10Dec 27, 2022
AFG2A20Jan 3, 2024
AFG3L264Oct 2, 2024
AGRN28Sep 13, 2021
AHI11Sep 25, 2019
AIFM12Sep 25, 2019
AIRE21Sep 13, 2021
AKT21Dec 30, 2022
ALDH7A16Dec 30, 2020
ALG1317Sep 13, 2021
ALG142Dec 30, 2022
ALG14-AS11Dec 30, 2022
ALG95Dec 27, 2022
ALMS125Dec 30, 2020
ALPL18Jan 3, 2024
ALS255Jan 3, 2024
AMT6Dec 30, 2020
ANAPC152Sep 25, 2019
ANG6Sep 13, 2021
ANGPT21Aug 31, 2018
ANKH3Dec 30, 2020
ANKRD1154Jan 3, 2024
ANO1075Jan 3, 2024
ANO552Jan 3, 2024
ANOS16Dec 30, 2020
AP5Z169Jan 3, 2024
APOB1Aug 17, 2017
APP34Oct 2, 2024
APTX28Jan 3, 2024
AQP24Aug 31, 2018
ARFGEF1-DT4Dec 30, 2020
ARFGEF215Sep 13, 2021
ARHGEF94Dec 27, 2022
ARID1A1Dec 30, 2022
ARMS25Aug 31, 2018
ARSA8Dec 27, 2022
ARSL1Dec 30, 2022
ARX5Dec 30, 2022
ASAH115Dec 27, 2022
ASPM85Jan 3, 2024
ASTN212Dec 27, 2022
ASXL11Dec 30, 2022
ATL123Jan 3, 2024
ATM227Oct 2, 2024
ATP13A232Sep 13, 2021
ATP1A245Jan 3, 2024
ATP1A317Dec 27, 2022
ATP2A134Jan 3, 2024
ATP2A1-AS11Aug 31, 2018
ATP2A28Sep 25, 2019
ATP2B27Dec 30, 2020
ATP6AP24Sep 25, 2019
ATP6V0A212Jan 3, 2024
ATP6V1B15Dec 30, 2020
ATP6V1B1-AS11Aug 31, 2018
ATP6V1B21Sep 25, 2019
ATP7A2Dec 30, 2022
ATRIP10Sep 25, 2019
ATRIP-TREX110Sep 25, 2019
ATRX15Dec 30, 2020
AVPR213Jan 3, 2024
AXDND110Jan 3, 2024
B3GNT41Dec 30, 2020
B4GAT11Aug 31, 2018
BAG38Jan 3, 2024
BBS17Sep 25, 2019
BBS103Aug 17, 2017
BBS23Jan 3, 2024
BCKDK9Dec 27, 2022
BCS1L2Sep 25, 2019
BDP113Sep 13, 2021
BICD25Jan 3, 2024
BIN13Dec 30, 2020
BRAT139Dec 30, 2020
BSCL222Jan 3, 2024
BSND4Sep 13, 2021
C10orf1054Dec 30, 2020
C11orf6587Oct 2, 2024
C12orf435Jan 3, 2024
C17orf10712Jan 3, 2024
CABP21Sep 25, 2019
CACNA1A330Oct 2, 2024
CACNA1D11Dec 30, 2022
CACNA1H144Jan 3, 2024
CACNA1S69Jan 3, 2024
CACNA2D112Sep 25, 2019
CACNA2D1-AS12Aug 17, 2017
CACNA2D213Dec 30, 2020
CACNB447Jan 3, 2024
CAPN389Jan 3, 2024
CASD131Jan 3, 2024
CASK3Dec 30, 2020
CASR114Jan 3, 2024
CATIP-AS25Aug 31, 2018
CAV322Jan 3, 2024
CAVIN15Dec 27, 2022
CC2D2A2Aug 17, 2017
CCDC504Sep 25, 2019
CCDC7812Sep 13, 2021
CCDC88C18Sep 13, 2021
CCM216Jan 3, 2024
CCNF1Sep 25, 2019
CDAN12Dec 30, 2022
CDC14A2Sep 25, 2019
CDH2338Dec 27, 2022
CDH23-AS11Sep 25, 2019
CDKL58Dec 30, 2020
CEACAM164Dec 30, 2020
CEACAM16-AS14Dec 30, 2020
CEMIP16Dec 27, 2022
CEP2903Dec 30, 2020
CFTR1Dec 30, 2022
CHAT8Dec 30, 2020
CHD224Dec 27, 2022
CHD725Jan 3, 2024
CHKB4Aug 31, 2018
CHKB-CPT1B4Aug 31, 2018
CHMP2B12Jan 3, 2024
CHRNA18Jan 3, 2024
CHRNA29Dec 27, 2022
CHRNA426Dec 27, 2022
CHRNA71Dec 27, 2022
CHRNB14Dec 30, 2022
CHRNB214Dec 30, 2020
CHRND5Jan 3, 2024
CHRNE18Jan 3, 2024
CHSY113Dec 30, 2020
CIB22Sep 25, 2019
CISD21Sep 25, 2019
CIZ11Aug 31, 2018
CLCC11Sep 25, 2019
CLCN1163Oct 2, 2024
CLCNKA13Aug 31, 2018
CLCNKB38Dec 27, 2022
CLDN145Sep 25, 2019
CLDN14-AS15Sep 25, 2019
CLIC53Sep 25, 2019
CLN37Dec 30, 2020
CLN512Jan 3, 2024
CLN610Sep 13, 2021
CLN89Dec 30, 2020
CLPP4Sep 25, 2019
CLRN12Dec 30, 2020
CNTN16Dec 30, 2020
CNTNAP11Dec 30, 2022
CNTNAP232Dec 27, 2022
COCH2Jan 3, 2024
COG41Dec 30, 2022
COL11A111Dec 30, 2022
COL11A29Sep 13, 2021
COL18A132Aug 31, 2018
COL1A183Jan 3, 2024
COL1A245Jan 3, 2024
COL2A115Dec 30, 2020
COL4A163Jan 3, 2024
COL4A21Sep 13, 2021
COL4A367Jan 3, 2024
COL4A485Dec 27, 2022
COL4A584Jan 3, 2024
COL4A67Dec 30, 2020
COL5A21Dec 30, 2022
COL6A120Dec 30, 2020
COL6A223Dec 30, 2020
COL6A352Dec 27, 2022
COL7A11Dec 30, 2022
COL9A110Dec 30, 2020
COL9A215Dec 30, 2020
COL9A315Jan 3, 2024
COLQ6Sep 13, 2021
COQ22Dec 30, 2022
COQ8A111Oct 2, 2024
CPA68Dec 30, 2020
CPAP16Jan 3, 2024
CPLANE11Aug 31, 2018
CPT214Jan 3, 2024
CREBBP1Dec 30, 2022
CRH4Sep 13, 2021
CRPPA14Dec 27, 2022
CRPPA-AS14Dec 30, 2020
CRYAB3Dec 30, 2020
CRYM1Sep 25, 2019
CSTB11Jan 3, 2024
CTSD9Sep 25, 2019
CTSF15Dec 30, 2020
CTXN2-AS18Sep 13, 2021
CUBN2Dec 30, 2022
CUL4B7Sep 25, 2019
CYB561D27Dec 30, 2020
CYP11B145Oct 2, 2024
CYP17A13Aug 31, 2018
CYP21A255Jan 3, 2024
CYP27A119Jan 3, 2024
CYP7B120Jan 3, 2024
DAG132Jan 3, 2024
DCDC25Sep 13, 2021
DCTN132Oct 2, 2024
DCX2Sep 25, 2019
DEAF114Dec 27, 2022
DEPDC529Dec 27, 2022
DES35Jan 3, 2024
DGUOK1Aug 17, 2017
DGUOK-AS11Aug 17, 2017
DHCR78Sep 13, 2021
DIABLO1Dec 30, 2020
DIAPH15Dec 30, 2020
DIAPH37Dec 30, 2020
DLX51Dec 30, 2020
DM1-AS1Sep 25, 2019
DMAC2L3Sep 13, 2021
DMD265Oct 2, 2024
DNAJB612Dec 27, 2022
DNAJC53Sep 25, 2019
DNM17Sep 25, 2019
DNM256Jan 3, 2024
DNMT13Sep 13, 2021
DOCK719Jan 3, 2024
DOCK81Dec 30, 2022
DOK714Jan 3, 2024
DPAGT13Dec 30, 2020
DPM21Dec 30, 2020
DPYD22Dec 27, 2022
DPYD-AS15Dec 30, 2020
DSP1Dec 30, 2022
DSPP11Dec 30, 2020
DYNC1H164Jan 3, 2024
DYRK1A6Sep 25, 2019
DYSF152Oct 2, 2024
ECHS12Dec 30, 2022
EDN31Sep 25, 2019
EDNRB5Sep 13, 2021
EDNRB-AS14Sep 13, 2021
EEF1A29Dec 30, 2020
EEF2112Jan 3, 2024
EFHC123Dec 27, 2022
EGILA6Sep 13, 2021
EGR218Jan 3, 2024
EIF2B33Dec 30, 2020
EIF2B45Aug 31, 2018
EIF2B54Jan 3, 2024
ELMOD36Sep 13, 2021
EMD6Jan 3, 2024
EMX24Sep 25, 2019
EMX2OS1Aug 17, 2017
EPM2A16Dec 27, 2022
EPM2A-DT5Sep 13, 2021
EPS86Sep 25, 2019
EPS8L25Dec 30, 2020
ERCC26Sep 25, 2019
ERCC33Sep 25, 2019
ESPN3Dec 30, 2020
ESR110Jan 3, 2024
ESR26Dec 30, 2020
ESRRB5Dec 30, 2020
ETHE11Dec 30, 2022
EYA13Sep 25, 2019
EYA41Sep 25, 2019
F13A11Dec 30, 2022
FA2H14Jan 3, 2024
FAM131B1Dec 27, 2022
FANCI9Jan 3, 2024
FBXL36Jan 3, 2024
FGD17Sep 25, 2019
FGD429Dec 27, 2022
FGF1423Jan 3, 2024
FGF233Sep 25, 2019
FGF32Sep 25, 2019
FGF81Aug 31, 2018
FGFR111Dec 27, 2022
FGFR26Dec 30, 2020
FGFR321Sep 13, 2021
FHL110Dec 27, 2022
FIG457Jan 3, 2024
FKBP142Dec 30, 2022
FKBP14-AS12Dec 30, 2022
FKRP30Jan 3, 2024
FKTN19Dec 27, 2022
FLNA30Jan 3, 2024
FLNC43Jan 3, 2024
FLNC-AS118Sep 13, 2021
FLVCR152Jan 3, 2024
FOLR12Sep 25, 2019
FOXC21Dec 30, 2022
FOXG19Dec 30, 2020
FOXI14Sep 25, 2019
FOXP31Dec 30, 2022
FTCD4Aug 31, 2018
FUS22Jan 3, 2024
FXN40Jan 3, 2024
GAA2Dec 30, 2022
GABRA16Sep 13, 2021
GABRB26Sep 25, 2019
GABRB38Sep 25, 2019
GABRD13Sep 25, 2019
GABRG214Sep 13, 2021
GAMT7Sep 13, 2021
GARS141Jan 3, 2024
GATA32Dec 30, 2020
GATAD13Dec 30, 2022
GATM4Dec 30, 2020
GBA12Dec 30, 2022
GCH120Dec 27, 2022
GCK242Oct 2, 2024
GDAP116Jan 3, 2024
GFAP31Jan 3, 2024
GFPT14Dec 30, 2020
GH-LCR144Jan 3, 2024
GH15Sep 25, 2019
GHR5Sep 13, 2021
GIPC32Sep 25, 2019
GJB184Jan 3, 2024
GJB280Jan 3, 2024
GJB38Sep 25, 2019
GJC22Sep 13, 2021
GJD2-DT1Dec 30, 2022
GLA1Dec 30, 2022
GLDC35Dec 30, 2022
GLUD110Sep 25, 2019
GML10Dec 30, 2020
GMPPB2Dec 30, 2022
GNAI31Dec 30, 2022
GNAO18Aug 31, 2018
GNAO1-AS11Aug 31, 2018
GNE7Sep 13, 2021
GNG31Aug 17, 2017
GNRH11Aug 31, 2018
GNRHR3Jan 3, 2024
GOSR26Dec 30, 2020
GPC35Dec 30, 2020
GPSM29Dec 30, 2020
GRHL24Sep 25, 2019
GRIA37Dec 27, 2022
GRIN111Dec 30, 2022
GRIN2A17Sep 13, 2021
GRIN2B20Sep 13, 2021
GRM1100Jan 3, 2024
GRN58Jan 3, 2024
GRXCR12Sep 25, 2019
GRXCR23Sep 25, 2019
GSDME3Jan 3, 2024
GTF3C2-AS23Aug 31, 2018
HADH1Dec 30, 2022
HADHB1Dec 30, 2022
HCN19Sep 13, 2021
HCN429Dec 30, 2020
HGF2Dec 30, 2020
HNF1A143Oct 2, 2024
HNF1B46Jan 3, 2024
HNF4A82Jan 3, 2024
HNRNPU7Sep 13, 2021
HNRNPUL2-BSCL222Jan 3, 2024
HOMER27Dec 30, 2020
HOXB13Sep 25, 2019
HPGD1Dec 30, 2022
HRAS1Dec 30, 2022
HSD11B29Sep 13, 2021
HSD17B410Dec 30, 2022
HSD3B25Jan 3, 2024
HSPB135Jan 3, 2024
HSPB34Aug 31, 2018
HSPB814Dec 27, 2022
HSPD113Jan 3, 2024
HSPG2301Jan 3, 2024
HTRA124Jan 3, 2024
IFIH11Dec 30, 2022
IGHMBP223Dec 27, 2022
ILDR15Sep 25, 2019
INF230Dec 27, 2022
INS8Dec 30, 2020
INS-IGF25Aug 31, 2018
IQSEC27Dec 30, 2020
ITGA710Dec 27, 2022
ITGBL14Sep 13, 2021
ITPR1215Jan 3, 2024
JAG11Dec 30, 2022
KAAG11Dec 30, 2020
KANSL127Dec 27, 2022
KARS14Sep 25, 2019
KBTBD136Sep 13, 2021
KCNA132Jan 3, 2024
KCNA25Sep 25, 2019
KCNB15Aug 31, 2018
KCNC18Jan 3, 2024
KCNC352Jan 3, 2024
KCND362Jan 3, 2024
KCNE11Sep 25, 2019
KCNH230Dec 27, 2022
KCNJ17Dec 30, 2020
KCNJ108Dec 30, 2020
KCNJ1129Jan 3, 2024
KCNJ24Sep 25, 2019
KCNMA123Jan 3, 2024
KCNMA1-AS17Dec 27, 2022
KCNQ16Jan 3, 2024
KCNQ1-AS11Sep 25, 2019
KCNQ222Oct 2, 2024
KCNQ312Dec 30, 2020
KCNQ45Sep 25, 2019
KCNT142Jan 3, 2024
KCTD77Dec 30, 2020
KDM5C3Dec 30, 2020
KDM6A1Dec 30, 2022
KIF1A70Jan 3, 2024
KIF5A26Oct 2, 2024
KIFBP11Jan 3, 2024
KIRREL23Sep 13, 2021
KISS1R5Sep 13, 2021
KLHL4011Sep 13, 2021
KLHL91Sep 13, 2021
KMT2D62Dec 30, 2022
KRIT115Jan 3, 2024
KRT11Dec 30, 2022
L1CAM19Jan 3, 2024
L2HGDH15Sep 13, 2021
LAMA291Oct 2, 2024
LAMB216Sep 13, 2021
LARGE117Sep 13, 2021
LARS12Dec 30, 2022
LARS212Jan 3, 2024
LARS2-AS16Jan 3, 2024
LBR14Dec 30, 2020
LDB314Dec 27, 2022
LDLR12Aug 31, 2018
LDLRAD220Dec 27, 2022
LEPR14Sep 13, 2021
LGI14Dec 30, 2020
LHCGR9Dec 27, 2022
LIAS6Dec 27, 2022
LITAF8Jan 3, 2024
LMNA55Jan 3, 2024
LMNB214Jan 3, 2024
LOC1001305873Sep 13, 2021
LOC1005060711Dec 30, 2020
LOC10192705521Dec 27, 2022
LOC10192800827Jan 3, 2024
LOC1019289651Sep 25, 2019
LOC1019293053Dec 30, 2020
LOC10272405843Jan 3, 2024
LOC10536914910Dec 27, 2022
LOC10537156612Sep 13, 2021
LOC10650171213Aug 31, 2018
LOC10650171334Dec 27, 2022
LOC1066279812Dec 30, 2022
LOC10678080053Jan 3, 2024
LOC10679983336Oct 2, 2024
LOC1070753171Sep 25, 2019
LOC1073033402Dec 30, 2020
LOC10765244518Dec 27, 2022
LOC1079822342Jul 17, 2017
LOC1080218461Dec 30, 2022
LOC1089031483Aug 31, 2018
LOC1096106311Sep 13, 2021
LOC1101212696Sep 13, 2021
LOC1101214864Dec 27, 2022
LOC1106739722Aug 17, 2017
LOC1118119673Aug 17, 2017
LOC1125336712Aug 31, 2018
LOC1128409212Sep 25, 2019
LOC1128722992Jan 3, 2024
LOC1136338771Dec 30, 2022
LOC1138395161Aug 31, 2018
LOC1138457882Aug 31, 2018
LOC1220948441Sep 25, 2019
LOC1221522962Dec 30, 2020
LOC1227871371Sep 25, 2019
LOC1238640653Dec 30, 2020
LOC1239562101Aug 31, 2018
LOC1239562577Dec 27, 2022
LOC1251774895Dec 30, 2020
LOC1254677682Dec 30, 2020
LOC1266533981Sep 25, 2019
LOC1268055761Sep 13, 2021
LOC1268056559Jan 3, 2024
LOC1268056883Dec 27, 2022
LOC1268058141Sep 25, 2019
LOC1268058773Sep 25, 2019
LOC1268058903Jan 3, 2024
LOC1268062521Sep 25, 2019
LOC1268063732Sep 13, 2021
LOC12680642010Dec 27, 2022
LOC1268064219Dec 27, 2022
LOC12680642213Dec 27, 2022
LOC1268064239Sep 13, 2021
LOC12680642413Jan 3, 2024
LOC12680642514Jan 3, 2024
LOC1268064266Dec 27, 2022
LOC12680642710Dec 27, 2022
LOC12680642813Sep 13, 2021
LOC1268064298Dec 27, 2022
LOC12680643010Sep 13, 2021
LOC1268064317Dec 27, 2022
LOC1268064337Jan 3, 2024
LOC1268065731Sep 25, 2019
LOC1268065834Jan 3, 2024
LOC12680659013Jan 3, 2024
LOC1268068781Aug 31, 2018
LOC1268069135Dec 27, 2022
LOC1268072387Sep 13, 2021
LOC1268598211Sep 13, 2021
LOC1268598368Jan 3, 2024
LOC12685983715Jan 3, 2024
LOC1268598387Jan 3, 2024
LOC1268601302Sep 25, 2019
LOC1268601314Dec 30, 2020
LOC1268602161Aug 31, 2018
LOC1268604032Sep 25, 2019
LOC1268604611Sep 25, 2019
LOC1268604983Sep 25, 2019
LOC1268605314Dec 27, 2022
LOC1268607824Jan 3, 2024
LOC1268611092Aug 31, 2018
LOC1268612451Jul 17, 2017
LOC1268613602Dec 30, 2020
LOC1268615093Dec 30, 2020
LOC1268615202Dec 30, 2022
LOC1268615352Dec 27, 2022
LOC1268616382Aug 17, 2017
LOC1268618972Jan 3, 2024
LOC1268618981Sep 25, 2019
LOC12686201920Jan 3, 2024
LOC1268620602Aug 31, 2018
LOC1268621151Sep 25, 2019
LOC1268621942Dec 30, 2020
LOC1268622782Aug 31, 2018
LOC1268622792Sep 25, 2019
LOC1268623616Dec 27, 2022
LOC1268624021Sep 25, 2019
LOC1268625001Sep 13, 2021
LOC12686254911Jan 3, 2024
LOC1268625781Aug 31, 2018
LOC1268625867Dec 30, 2022
LOC1268627571Aug 31, 2018
LOC1268628647Jan 3, 2024
LOC1268628654Dec 30, 2020
LOC1268628661Sep 13, 2021
LOC1268629024Dec 30, 2020
LOC1268630843Dec 30, 2020
LOC1268630872Sep 25, 2019
LOC1268631452Sep 25, 2019
LOC1268632071Dec 30, 2022
LOC1278142973Sep 25, 2019
LOC1278985647Dec 30, 2020
LOC1299292411Dec 30, 2020
LOC1299295401Sep 25, 2019
LOC1299304461Dec 30, 2022
LOC1299305611Aug 31, 2018
LOC1299306551Aug 31, 2018
LOC1299315974Sep 13, 2021
LOC1299321551Aug 31, 2018
LOC1299324867Jan 3, 2024
LOC1299333341Sep 25, 2019
LOC1299342361Aug 31, 2018
LOC1299349256Sep 13, 2021
LOC1299351836Jan 3, 2024
LOC1299351841Sep 25, 2019
LOC1299351851Sep 25, 2019
LOC1299351861Aug 17, 2017
LOC1299357302Dec 27, 2022
LOC1299925852Sep 25, 2019
LOC12999281313Sep 13, 2021
LOC1299928921Sep 25, 2019
LOC1299942051Aug 31, 2018
LOC1299954492Aug 31, 2018
LOC1299973815Sep 13, 2021
LOC1299974805Dec 30, 2020
LOC1299978612Sep 13, 2021
LOC1299980054Dec 27, 2022
LOC1299983953Jan 3, 2024
LOC1299985333Dec 30, 2020
LOC1299992731Sep 13, 2021
LOC1299999401Aug 31, 2018
LOC1300005231Sep 13, 2021
LOC1300006222Sep 25, 2019
LOC1300013343Jan 3, 2024
LOC1300013384Dec 30, 2020
LOC1300013422Sep 13, 2021
LOC1300016813Dec 30, 2020
LOC13000186217Jan 3, 2024
LOC1300026511Aug 17, 2017
LOC1300030931Sep 25, 2019
LOC1300032781Dec 30, 2020
LOC1300039591Dec 30, 2020
LOC1300042541Sep 25, 2019
LOC1300072181Dec 30, 2020
LOC1300093664Dec 27, 2022
LOC1300097473Dec 27, 2022
LOC1300099131Aug 31, 2018
LOC1300556924Aug 31, 2018
LOC1300567093Jan 3, 2024
LOC1300569731Aug 17, 2017
LOC1300580682Aug 31, 2018
LOC1300591561Aug 17, 2017
LOC1300593943Dec 30, 2020
LOC1300598187Jan 3, 2024
LOC1300600402Jan 3, 2024
LOC1300600411Aug 31, 2018
LOC1300601471Dec 30, 2022
LOC1300619401Sep 13, 2021
LOC1300620841Sep 25, 2019
LOC1300629451Sep 25, 2019
LOC1300630651Sep 25, 2019
LOC1300630661Aug 17, 2017
LOC13006316912Jan 3, 2024
LOC1300638073Dec 27, 2022
LOC1300644543Sep 13, 2021
LOC1300645431Aug 17, 2017
LOC1300653454Sep 25, 2019
LOC1300667883Dec 27, 2022
LOC1300678622Aug 31, 2018
LOC1300678641Aug 17, 2017
LOC1300683392Sep 13, 2021
LOC1300686212Dec 30, 2020
LOC1300687461Aug 31, 2018
LOC1320905951Aug 31, 2018
LOXHD123Dec 30, 2020
LRP59Dec 27, 2022
LRRC37A26Dec 30, 2020
LRRC511Sep 25, 2019
LRRC561Dec 30, 2022
LRRK231Jan 3, 2024
LRTOMT4Sep 25, 2019
LZTR12Oct 2, 2024
MAF6Dec 27, 2022
MAGI218Dec 27, 2022
MAGI2-AS32Sep 25, 2019
MANBA4Dec 30, 2020
MAP4K51Sep 13, 2021
MAPT25Oct 2, 2024
MARVELD24Sep 13, 2021
MATR32Aug 17, 2017
MBD515Dec 27, 2022
MC4R13Jan 3, 2024
MCM28Jan 3, 2024
MCOLN13Sep 13, 2021
MCPH125Sep 13, 2021
MCPH1-AS18Sep 13, 2021
ME23Aug 17, 2017
MECP222Jan 3, 2024
MED121Dec 30, 2022
MEF2C1Jan 3, 2024
MEF2C-AS21Jan 3, 2024
MEGF1010Dec 27, 2022
MEN116Jan 3, 2024
MESD1Sep 25, 2019
MET6Sep 25, 2019
MFF-DT65Jan 3, 2024
MFN283Oct 2, 2024
MFSD84Sep 13, 2021
MHRT6Jan 3, 2024
MID11Dec 30, 2022
MIF4GD-DT2Aug 31, 2018
MINK11Aug 31, 2018
MIR3936HG2Dec 30, 2020
MIR60842Aug 31, 2018
MIR6511B13Dec 27, 2022
MIR67661Dec 30, 2020
MIR962Sep 25, 2019
MITF6Dec 30, 2020
MMACHC2Dec 30, 2022
MPDZ1Dec 30, 2022
MPV172Dec 27, 2022
MPZ60Jan 3, 2024
MRE1163Jan 3, 2024
MSRB31Dec 30, 2020
MT-CO126Sep 13, 2021
MT-CO211Dec 30, 2020
MT-ND119Sep 13, 2021
MT-RNR113Jan 3, 2024
MT-TI1Sep 25, 2019
MT-TK2Jan 3, 2024
MT-TQ2Dec 30, 2020
MT-TS11Sep 25, 2019
MT-TS22Dec 30, 2020
MTM13Dec 30, 2022
MTMR220Jan 3, 2024
MTPAP38Jan 3, 2024
MUSK10Jan 3, 2024
MVP-DT14Jan 3, 2024
MYBPC311Jan 3, 2024
MYH111Aug 17, 2017
MYH1424Sep 13, 2021
MYH26Sep 13, 2021
MYH720Jan 3, 2024
MYH913Dec 27, 2022
MYHAS6Sep 13, 2021
MYO15A28Jan 3, 2024
MYO3A10Dec 30, 2020
MYO69Sep 25, 2019
MYO7A29Jan 3, 2024
MYOT21Dec 27, 2022
NALCN1Dec 30, 2022
NARS26Jan 3, 2024
NDE16Jan 3, 2024
NDP1Sep 25, 2019
NDP-AS11Sep 25, 2019
NDRG125Jan 3, 2024
NDUFA12Dec 30, 2020
NDUFAF51Dec 30, 2022
NDUFB31Dec 30, 2022
NEB114Jan 3, 2024
NEFL26Jan 3, 2024
NEXMIF10Sep 25, 2019
NF185Oct 2, 2024
NF212Dec 27, 2022
NHLRC18Jan 3, 2024
NICN11Sep 25, 2019
NIPA19Jan 3, 2024
NIPBL21Dec 27, 2022
NKX2-11Dec 30, 2022
NKX2-51Dec 30, 2022
NLRP312Dec 30, 2022
NOC3L2Aug 17, 2017
NOTCH3479Jan 3, 2024
NPC12Dec 30, 2022
NPHS142Dec 30, 2022
NPHS229Jan 3, 2024
NR0B18Dec 30, 2020
NR2F12Aug 31, 2018
NR2F1-AS11Aug 31, 2018
NR3C22Dec 30, 2022
NRXN119Sep 13, 2021
NSD11Dec 30, 2022
NTRK118Sep 13, 2021
OFD18Sep 13, 2021
OPA192Jan 3, 2024
OPA1-AS12Aug 31, 2018
OPHN19Dec 30, 2020
OPTN16Jan 3, 2024
OSBPL25Sep 13, 2021
OTC1Dec 30, 2022
OTOA5Jan 3, 2024
OTOF33Jan 3, 2024
OTOG41Jan 3, 2024
OTOGL11Dec 30, 2020
OTOP21Sep 25, 2019
OXTR15Jan 3, 2024
P2RX24Dec 30, 2020
PACRG1Sep 25, 2019
PAFAH1B11Aug 31, 2018
PAK33Sep 25, 2019
PANK29Dec 30, 2020
PARK78Jan 3, 2024
PAX33Dec 30, 2020
PCCB2Dec 30, 2022
PCDH1524Jan 3, 2024
PCDH1924Oct 2, 2024
PDCD101Aug 17, 2017
PDHA13Dec 27, 2022
PDX134Jan 3, 2024
PDYN29Jan 3, 2024
PDYN-AS129Jan 3, 2024
PDZD713Dec 30, 2020
PEX112Dec 30, 2022
PEX611Dec 30, 2022
PEX76Jan 3, 2024
PFN11Sep 25, 2019
PHEX28Jan 3, 2024
PHEX-AS11Aug 31, 2018
PHF61Dec 27, 2022
PHGDH7Dec 30, 2020
PHKA21Dec 30, 2022
PI4KA1Aug 31, 2018
PIGA3Sep 25, 2019
PIGN18Jan 3, 2024
PIGO15Jan 3, 2024
PIGV2Sep 13, 2021
PINK120Jan 3, 2024
PINK1-AS13Jan 3, 2024
PJVK1Sep 25, 2019
PKD1525Oct 2, 2024
PKD1-AS154Dec 27, 2022
PKD264Jan 3, 2024
PKD2L2-DT21Dec 27, 2022
PKP21Dec 30, 2022
PLA2G611Sep 13, 2021
PLCB117Sep 25, 2019
PLCE123Dec 30, 2020
PLCE1-AS11Sep 25, 2019
PLD31Jul 17, 2017
PLEC377Jan 3, 2024
PLP16Jan 3, 2024
PLUT9Sep 13, 2021
PMP2230Oct 2, 2024
PNKD5Aug 31, 2018
PNKP13Sep 25, 2019
PNPLA644Jan 3, 2024
PNPO8Dec 30, 2022
PNPT15Dec 30, 2022
POLG189Jan 3, 2024
POLGARF189Jan 3, 2024
POLR1C3Dec 30, 2020
POLR1D5Sep 25, 2019
POLR2F4Dec 27, 2022
POMGNT124Dec 27, 2022
POMGNT25Dec 30, 2022
POMT158Jan 3, 2024
POMT236Jan 3, 2024
POU1F11Aug 31, 2018
POU4F33Sep 25, 2019
PPT14Dec 30, 2020
PQBP12Aug 31, 2018
PRADX4Sep 25, 2019
PRICKLE117Dec 30, 2020
PRICKLE217Dec 27, 2022
PRICKLE2-AS11Dec 27, 2022
PRIMA15Sep 25, 2019
PRKCG73Jan 3, 2024
PRKN18Jan 3, 2024
PROK22Dec 27, 2022
PROKR26Dec 30, 2022
PROP15Aug 31, 2018
PRPS11Dec 30, 2020
PRRT214Jan 3, 2024
PRX77Jan 3, 2024
PSEN150Jan 3, 2024
PSEN227Dec 27, 2022
PTCHD1-AS8Jan 3, 2024
PTEN1Aug 31, 2018
PTPN117Dec 30, 2022
PTPRQ19Dec 30, 2020
PURA1Sep 25, 2019
QARS18Sep 13, 2021
RAB33A2Sep 25, 2019
RAB39B1Dec 30, 2020
RAB3GAP116Jan 3, 2024
RAB7A8Jan 3, 2024
RAB9B6Jan 3, 2024
RAF11Dec 30, 2022
RAI129Jan 3, 2024
RAPSN8Sep 13, 2021
RARS22Dec 30, 2022
RBFOX110Sep 13, 2021
RDX3Dec 30, 2020
REEP114Jan 3, 2024
RELN66Jan 3, 2024
RET23Jan 3, 2024
RIF123Jan 3, 2024
RIPOR221Dec 27, 2022
RNASE46Sep 13, 2021
RNASEH2A5Sep 25, 2019
RNASEH2B7Sep 25, 2019
RNASEH2C2Sep 13, 2021
RNF173Sep 13, 2021
RNR11Sep 25, 2019
ROGDI12Sep 25, 2019
ROR13Sep 25, 2019
RPL36A-HNRNPH21Dec 30, 2022
RRM2B2Sep 25, 2019
RS13Dec 30, 2020
RTN227Jan 3, 2024
RXYLT15Sep 13, 2021
RXYLT1-AS11Aug 31, 2018
RYR179Jan 3, 2024
S1PR23Dec 30, 2020
SACS368Jan 3, 2024
SALL18Dec 30, 2020
SAMHD12Aug 31, 2018
SBF277Jan 3, 2024
SBF2-AS117Jan 3, 2024
SCARB29Dec 30, 2020
SCN1A94Jan 3, 2024
SCN1A-AS134Jan 3, 2024
SCN1B9Sep 13, 2021
SCN2A41Jan 3, 2024
SCN3A21Dec 27, 2022
SCN4A204Jan 3, 2024
SCN5A49Jan 3, 2024
SCN8A19Dec 30, 2022
SCN9A41Jan 3, 2024
SCNN1B26Jan 3, 2024
SCNN1G14Sep 13, 2021
SCO23Sep 25, 2019
SDHB5Jan 3, 2024
SELENON16Dec 27, 2022
SEMA3E5Sep 13, 2021
SEPTIN99Dec 30, 2020
SERPINB64Dec 30, 2020
SERPINI14Sep 25, 2019
SETBP114Dec 27, 2022
SETD218Dec 30, 2020
SETX282Jan 3, 2024
SFTA31Dec 30, 2022
SGCA23Jan 3, 2024
SGCB14Dec 27, 2022
SGCD13Jan 3, 2024
SGCE33Jan 3, 2024
SGCG21Jan 3, 2024
SH3TC277Jan 3, 2024
SHANK21Aug 31, 2018
SHANK31Aug 31, 2018
SHH5Sep 25, 2019
SHLD21Aug 31, 2018
SHOC21Dec 30, 2022
SHOX67Jan 3, 2024
SIGMAR16Sep 13, 2021
SIK118Dec 27, 2022
SIL157Jan 3, 2024
SIX11Sep 25, 2019
SIX310Dec 30, 2022
SIX54Sep 13, 2021
SLC12A124Dec 27, 2022
SLC12A361Dec 27, 2022
SLC13A56Jan 3, 2024
SLC17A83Dec 30, 2020
SLC19A112Aug 31, 2018
SLC19A22Sep 25, 2019
SLC19A313Dec 30, 2020
SLC1A354Jan 3, 2024
SLC22A43Dec 30, 2020
SLC25A195Sep 25, 2019
SLC25A2210Jan 3, 2024
SLC25A43Dec 27, 2022
SLC26A410Dec 30, 2020
SLC26A4-AS11Sep 25, 2019
SLC26A54Dec 27, 2022
SLC26A5-AS18Sep 13, 2021
SLC2A119Dec 27, 2022
SLC33A111Dec 27, 2022
SLC35A25Dec 30, 2020
SLC4A1010Dec 27, 2022
SLC4A1111Dec 30, 2020
SLC6A116Sep 13, 2021
SLC6A1-AS13Sep 25, 2019
SLC6A817Dec 30, 2022
SLC9A69Dec 30, 2020
SLITRK66Sep 25, 2019
SMARCA41Dec 30, 2022
SMC1A6Dec 30, 2020
SMC310Sep 13, 2021
SMCHD128Dec 27, 2022
SMN132Jan 3, 2024
SMS2Dec 30, 2020
SNAI21Sep 25, 2019
SNAP253Aug 31, 2018
SNAP296Aug 31, 2018
SNHG149Dec 27, 2022
SOD130Oct 2, 2024
SOD1-DT3Jan 3, 2024
SOS13Dec 30, 2022
SOX104Dec 27, 2022
SOX91Dec 30, 2022
SPART13Jan 3, 2024
SPAST135Jan 3, 2024
SPG1186Jan 3, 2024
SPG216Dec 27, 2022
SPG760Jan 3, 2024
SPTA11Dec 30, 2022
SPTAN134Dec 30, 2020
SPTBN2266Jan 3, 2024
SPTLC14Jan 3, 2024
SPTLC23Jan 3, 2024
SQSTM131Jan 3, 2024
SRPX25Sep 25, 2019
SSUH26Sep 13, 2021
ST3GAL35Sep 25, 2019
ST3GAL57Sep 13, 2021
STAR6Sep 25, 2019
STIL13Dec 30, 2020
STON1-GTF2A1L9Dec 27, 2022
STRC11Dec 30, 2020
STX1B6Sep 25, 2019
STXBP112Sep 13, 2021
SUCLA212Dec 27, 2022
SYN110Dec 30, 2020
SYNE1903Jan 3, 2024
SYNE1-AS110Jan 3, 2024
SYNE2155Jan 3, 2024
SYNE43Dec 30, 2020
SYNGAP18Jan 3, 2024
SYNGAP1-AS17Jan 3, 2024
SYNJ126Dec 27, 2022
SYP1Aug 31, 2018
SYT1435Jan 3, 2024
SZT245Jan 3, 2024
TACR33Sep 13, 2021
TACR3-AS12Sep 13, 2021
TAPBPL11Jan 3, 2024
TARDBP17Dec 27, 2022
TARID1Sep 25, 2019
TBC1D2420Jan 3, 2024
TBCEL-TECTA13Sep 13, 2021
TBL1XR18Dec 30, 2020
TBL1XR1-AS12Aug 31, 2018
TBX116Sep 13, 2021
TCAP10Dec 27, 2022
TCF411Sep 13, 2021
TCOF115Sep 13, 2021
TDP164Jan 3, 2024
TECTA13Sep 13, 2021
TFAP2A2Sep 25, 2019
TGM6130Aug 5, 2024
TH21Dec 30, 2020
THAP18Jan 3, 2024
TIA13Aug 17, 2017
TJP212Sep 13, 2021
TK22Dec 30, 2020
TMC110Dec 30, 2020
TMEM132E8Sep 13, 2021
TMEM2161Aug 17, 2017
TMEM439Jan 3, 2024
TMEM672Aug 17, 2017
TMEM702Dec 30, 2022
TMPRSS34Dec 30, 2020
TNC21Sep 13, 2021
TNNT11Sep 25, 2019
TNXB5Jan 3, 2024
TOMT2Sep 25, 2019
TPI11Dec 30, 2022
TPM22Dec 30, 2020
TPM32Sep 25, 2019
TPP122Dec 30, 2020
TPRN3Sep 25, 2019
TRAPPC1136Jan 3, 2024
TRAPPC2L1Aug 31, 2018
TREX110Sep 25, 2019
TRIM3212Dec 27, 2022
TRIOBP11Dec 30, 2020
TRPC619Dec 27, 2022
TRPV463Jan 3, 2024
TSC170Jan 3, 2024
TSC2214Jan 3, 2024
TSEN5421Dec 27, 2022
TSPAN122Dec 27, 2022
TSPEAR8Sep 25, 2019
TSPEAR-AS11Sep 25, 2019
TSR23Sep 25, 2019
TTBK289Jan 3, 2024
TTN1234Jan 3, 2024
TTN-AS1688Jan 3, 2024
TTPA28Jan 3, 2024
TTR35Jan 3, 2024
TUBA1A9Sep 13, 2021
TUBA87Sep 25, 2019
TUBB2B5Sep 25, 2019
TUBB66Dec 27, 2022
TWNK16Jan 3, 2024
TYMP5Sep 25, 2019
UBA13Sep 25, 2019
UBE3A9Dec 27, 2022
UBQLN29Sep 13, 2021
UGT1A1Dec 30, 2022
UGT1A11Dec 30, 2022
UGT1A101Dec 30, 2022
UGT1A31Dec 30, 2022
UGT1A41Dec 30, 2022
UGT1A51Dec 30, 2022
UGT1A61Dec 30, 2022
UGT1A71Dec 30, 2022
UGT1A81Dec 30, 2022
UGT1A91Dec 30, 2022
UMOD11Jan 3, 2024
USH1C5Sep 25, 2019
USH1G4Sep 25, 2019
USH2A47Sep 13, 2021
USH2A-AS13Sep 25, 2019
USH2A-AS22Sep 13, 2021
VAMP111Jan 3, 2024
VAPB7Dec 30, 2020
VCP19Jan 3, 2024
VHL5Dec 30, 2020
VPS13A56Jan 3, 2024
VPS13B59Jan 3, 2024
VRK11Aug 31, 2018
WASHC527Jan 3, 2024
WASHC5-AS11Dec 27, 2022
WDR454Oct 2, 2024
WDR6234Sep 25, 2019
WFS117Sep 13, 2021
WHRN11Sep 13, 2021
WNK124Jan 3, 2024
WT114Dec 30, 2022
WWOX28Jan 3, 2024
YARS117Oct 2, 2024
ZDHHC245Sep 25, 2019
ZEB210Dec 30, 2020
ZFYVE2681Jan 3, 2024
ZRANB32Aug 31, 2018

Condition

NameSubmissionsLast Updated
Adrenoleukodystrophy1Jul 17, 2017
Alzheimer disease 42Jul 17, 2017
Amyotrophic lateral sclerosis type 113Jul 17, 2017
Amyotrophic lateral sclerosis type 42Jul 17, 2017
Amyotrophic lateral sclerosis type 62Jul 17, 2017
Ateleiotic dwarfism2Jul 17, 2017
Autosomal dominant Alport syndrome8Jul 17, 2017
Autosomal dominant isolated somatotropin deficiency2Jul 17, 2017
Autosomal dominant nocturnal frontal lobe epilepsy 13Jul 17, 2017
Autosomal dominant nonsyndromic hearing loss 3A1Jul 17, 2017
Autosomal dominant optic atrophy classic form2Jul 17, 2017
Autosomal recessive Alport syndrome12Jul 17, 2017
Autosomal recessive distal spinal muscular atrophy 14Jul 17, 2017
Autosomal recessive early-onset Parkinson disease 61Jul 17, 2017
Autosomal recessive limb-girdle muscular dystrophy type 2A14Jul 17, 2017
Autosomal recessive limb-girdle muscular dystrophy type 2B9Jul 17, 2017
Autosomal recessive limb-girdle muscular dystrophy type 2C1Oct 6, 2015
Autosomal recessive limb-girdle muscular dystrophy type 2D1Oct 6, 2015
Autosomal recessive limb-girdle muscular dystrophy type 2E1Oct 6, 2015
Autosomal recessive limb-girdle muscular dystrophy type 2F1Jul 17, 2017
Autosomal recessive limb-girdle muscular dystrophy type 2I4Jul 17, 2017
Autosomal recessive limb-girdle muscular dystrophy type 2K6Jul 17, 2017
Autosomal recessive limb-girdle muscular dystrophy type 2L4Oct 6, 2015
Autosomal recessive limb-girdle muscular dystrophy type 2M1Jul 17, 2017
Autosomal recessive nonsyndromic hearing loss 1A1Jul 17, 2017
Bardet-Biedl syndrome 15Jul 17, 2017
Bardet-Biedl syndrome 101Jul 17, 2017
Bardet-Biedl syndrome 21Jul 17, 2017
Bartter disease type 4A1Jul 17, 2017
Becker muscular dystrophy7Jul 17, 2017
Bethlem myopathy 1A21Jul 17, 2017
Brain small vessel disease 1 with or without ocular anomalies10Jul 17, 2017
CARASIL syndrome4Jul 17, 2017
Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 12Jul 17, 2017
Charcot-Marie-Tooth disease X-linked dominant 12Oct 6, 2015
Charcot-Marie-Tooth disease axonal type 2C2Oct 6, 2015
Charcot-Marie-Tooth disease axonal type 2F1Oct 6, 2015
Charcot-Marie-Tooth disease axonal type 2K1Jul 17, 2017
Charcot-Marie-Tooth disease type 1B5Jul 17, 2017
Charcot-Marie-Tooth disease type 1C1Jul 17, 2017
Charcot-Marie-Tooth disease type 2A25Oct 6, 2015
Charcot-Marie-Tooth disease type 2B1Jul 17, 2017
Charcot-Marie-Tooth disease type 2B11Oct 6, 2015
Charcot-Marie-Tooth disease type 2D2Jul 17, 2017
Charcot-Marie-Tooth disease type 2I1Jul 17, 2017
Charcot-Marie-Tooth disease type 2J1Jul 17, 2017
Charcot-Marie-Tooth disease type 4A2Jul 17, 2017
Charcot-Marie-Tooth disease type 4B15Jul 17, 2017
Charcot-Marie-Tooth disease type 4C2Oct 6, 2015
Charcot-Marie-Tooth disease type 4F7Jul 17, 2017
Charcot-Marie-Tooth disease type 4J4Jul 17, 2017
Charcot-Marie-Tooth disease, type IA3Oct 6, 2015
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency1Jul 17, 2017
Cohen syndrome2Jul 17, 2017
Congenital myasthenic syndrome 1614Jul 17, 2017
Congenital myotonia, autosomal dominant form1Jul 17, 2017
Congenital myotonia, autosomal recessive form1Jul 17, 2017
Cortical dysplasia-focal epilepsy syndrome7Jul 17, 2017
Developmental and epileptic encephalopathy, 12Jul 17, 2017
Diabetes insipidus, nephrogenic, X-linked1Jul 17, 2017
Dilated cardiomyopathy 1A2Oct 6, 2015
Distal myopathy with anterior tibial onset1Jul 17, 2017
Distal myopathy, Tateyama type1Jul 17, 2017
Drash syndrome3Jul 17, 2017
Duchenne muscular dystrophy69Jul 17, 2017
Emery-Dreifuss muscular dystrophy 2, autosomal dominant4Oct 6, 2015
Encephalopathy due to GLUT1 deficiency2Jul 17, 2017
Episodic ataxia type 24Jul 17, 2017
Familial hyperkalemic periodic paralysis14Jul 17, 2017
Familial hypokalemia-hypomagnesemia10Jul 17, 2017
Familial juvenile hyperuricemic nephropathy type 12Jul 17, 2017
Familial partial lipodystrophy, Dunnigan type1Oct 6, 2015
Febrile seizures, familial, 82Jul 17, 2017
Finnish congenital nephrotic syndrome4Jul 17, 2017
Focal segmental glomerulosclerosis 14Jul 17, 2017
Focal segmental glomerulosclerosis 23Jul 17, 2017
Focal segmental glomerulosclerosis 52Jul 17, 2017
Frasier syndrome3Jul 17, 2017
GRN-related frontotemporal lobar degeneration with Tdp43 inclusions9Jul 17, 2017
Generalized epilepsy with febrile seizures plus, type 23Jul 17, 2017
Hereditary spastic paraplegia 115Jul 17, 2017
Hereditary spastic paraplegia 311Jul 17, 2017
Hereditary spastic paraplegia 3A2Jul 17, 2017
Hereditary spastic paraplegia 73Jul 17, 2017
Hereditary spastic paraplegia 83Jul 17, 2017
Hyperinsulinemic hypoglycemia, familial, 13Jul 17, 2017
Hyperinsulinemic hypoglycemia, familial, 25Jul 17, 2017
Hyperinsulinism-hyperammonemia syndrome2Jul 17, 2017
Hypogonadotropic hypogonadism 3 with or without anosmia3Jul 17, 2017
Hypokalemic periodic paralysis, type 17Jul 17, 2017
Hypokalemic periodic paralysis, type 214Jul 17, 2017
Intellectual disability, X-linked, with or without seizures, arx-related2Jul 17, 2017
Isolated growth hormone deficiency type IB2Jul 17, 2017
Juvenile myoclonic epilepsy7Jul 17, 2017
Lafora disease2Jul 17, 2017
Laron-type isolated somatotropin defect3Jul 17, 2017
Malignant hyperthermia, susceptibility to, 57Jul 17, 2017
Merosin deficient congenital muscular dystrophy10Jul 17, 2017
Metachromatic leukodystrophy3Jul 17, 2017
Microcephaly 2, primary, autosomal recessive, with or without cortical malformations10Jul 17, 2017
Migraine, familial hemiplegic, 14Jul 17, 2017
Migraine, familial hemiplegic, 21Jul 17, 2017
Migraine, familial hemiplegic, 33Jul 17, 2017
Miyoshi muscular dystrophy 11Jul 17, 2017
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 41Jul 17, 2017
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A16Jul 17, 2017
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A52Jul 17, 2017
Muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B16Jul 17, 2017
Muscular dystrophy-dystroglycanopathy (congenital without intellectual disability), type B41Jul 17, 2017
Muscular dystrophy-dystroglycanopathy type B52Jul 17, 2017
Myoclonic dystonia 112Jul 17, 2017
Myofibrillar myopathy 32Jul 17, 2017
Myofibrillar myopathy 64Jul 17, 2017
Nephrogenic syndrome of inappropriate antidiuresis1Jul 17, 2017
Nephrotic syndrome, type 22Jul 17, 2017
Nephrotic syndrome, type 43Jul 17, 2017
Neuronopathy, distal hereditary motor, type 5A2Jul 17, 2017
Neuropathy, hereditary sensory and autonomic, type 2A12Jul 17, 2017
Neuropathy, hereditary sensory, type 1D2Jul 17, 2017
Obesity due to leptin receptor gene deficiency1Jul 17, 2017
Paramyotonia congenita of Von Eulenburg14Jul 17, 2017
Paroxysmal nonkinesigenic dyskinesia 13Jul 17, 2017
Polycystic kidney disease, adult type24Jul 17, 2017
Potassium-aggravated myotonia14Jul 17, 2017
Rett syndrome4Oct 6, 2015
Rippling muscle disease 21Jul 17, 2017
Seizures, benign familial neonatal, 13Jul 17, 2017
Severe myoclonic epilepsy in infancy26Jul 17, 2017
Short stature due to growth hormone qualitative anomaly2Jul 17, 2017
Smith-Lemli-Opitz syndrome5Jul 17, 2017
Smith-Magenis syndrome6Jul 17, 2017
Spinocerebellar ataxia type 55Jul 17, 2017
Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 22Jul 17, 2017
Tuberous sclerosis 125Jul 17, 2017
Tuberous sclerosis 266Jul 17, 2017
Ullrich congenital muscular dystrophy 1A21Jul 17, 2017
Wilms tumor 13Jul 17, 2017
X-linked myopathy with postural muscle atrophy1Jul 17, 2017
X-linked scapuloperoneal muscular dystrophy1Jul 17, 2017
not provided14369Oct 2, 2024
not specified4815Dec 27, 2022

Testing in GTR

Disease nameNumber of tests
3 beta-Hydroxysteroid dehydrogenase deficiency1 test
ALG9 congenital disorder of glycosylation4 tests
Aarskog syndrome2 tests
Absence seizure2 tests
Achondroplasia2 tests
Actin accumulation myopathy1 test
Action myoclonus-renal failure syndrome2 tests
Adenylosuccinate lyase deficiency5 tests
Adrenoleukodystrophy3 tests
Adult-onset proximal spinal muscular atrophy, autosomal dominant1 test
Aicardi-Goutieres syndrome 12 tests
Aicardi-Goutieres syndrome 22 tests
Aicardi-Goutieres syndrome 32 tests
Aicardi-Goutieres syndrome 42 tests
Aicardi-Goutieres syndrome 52 tests
Alexander disease4 tests
Alternating hemiplegia of childhood 22 tests
Alzheimer disease2 tests
Alzheimer disease 21 test
Alzheimer disease 32 tests
Alzheimer disease 42 tests
Amelocerebrohypohidrotic syndrome2 tests
Amyloidosis, hereditary systemic 12 tests
Amyotrophic lateral sclerosis type 13 tests
Amyotrophic lateral sclerosis type 102 tests
Amyotrophic lateral sclerosis type 122 tests
Amyotrophic lateral sclerosis type 152 tests
Amyotrophic lateral sclerosis type 162 tests
Amyotrophic lateral sclerosis type 182 tests
Amyotrophic lateral sclerosis type 2, juvenile6 tests
Amyotrophic lateral sclerosis type 211 test
Amyotrophic lateral sclerosis type 45 tests
Amyotrophic lateral sclerosis type 62 tests
Amyotrophic lateral sclerosis type 82 tests
Amyotrophic lateral sclerosis type 92 tests
Amyotrophic neuralgia1 test
Andersen Tawil syndrome1 test
Anemia, nonspherocytic hemolytic, due to G6PD deficiency1 test
Angelman syndrome2 tests
Aniridia 12 tests
Apparent mineralocorticoid excess3 tests
Arginine:glycine amidinotransferase deficiency3 tests
Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia4 tests
Ataxia-hypogonadism-choroidal dystrophy syndrome3 tests
Ataxia-telangiectasia syndrome4 tests
Ataxia-telangiectasia-like disorder 13 tests
Ateleiotic dwarfism2 tests
Autism, susceptibility to, 171 test
Autosomal dominant Alport syndrome2 tests
Autosomal dominant Parkinson disease 13 tests
Autosomal dominant Parkinson disease 43 tests
Autosomal dominant Parkinson disease 83 tests
Autosomal dominant childhood-onset proximal spinal muscular atrophy with contractures1 test
Autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures1 test
Autosomal dominant hypocalcemia 11 test
Autosomal dominant hypophosphatemic rickets2 tests
Autosomal dominant isolated somatotropin deficiency2 tests
Autosomal dominant limb-girdle muscular dystrophy type 1D (DNAJB6)2 tests
Autosomal dominant nocturnal frontal lobe epilepsy 12 tests
Autosomal dominant nocturnal frontal lobe epilepsy 32 tests
Autosomal dominant nocturnal frontal lobe epilepsy 42 tests
Autosomal dominant nonsyndromic hearing loss 3A2 tests
Autosomal dominant nonsyndromic hearing loss 3B2 tests
Autosomal dominant optic atrophy classic form2 tests
Autosomal recessive Alport syndrome3 tests
Autosomal recessive DOPA responsive dystonia2 tests
Autosomal recessive ataxia due to ubiquinone deficiency3 tests
Autosomal recessive ataxia, Beauce type3 tests
Autosomal recessive distal spinal muscular atrophy 11 test
Autosomal recessive distal spinal muscular atrophy 22 tests
Autosomal recessive early-onset Parkinson disease 63 tests
Autosomal recessive early-onset Parkinson disease 73 tests
Autosomal recessive juvenile Parkinson disease 23 tests
Autosomal recessive limb-girdle muscular dystrophy type 2A4 tests
Autosomal recessive limb-girdle muscular dystrophy type 2B3 tests
Autosomal recessive limb-girdle muscular dystrophy type 2C3 tests
Autosomal recessive limb-girdle muscular dystrophy type 2D3 tests
Autosomal recessive limb-girdle muscular dystrophy type 2E2 tests
Autosomal recessive limb-girdle muscular dystrophy type 2F2 tests
Autosomal recessive limb-girdle muscular dystrophy type 2G3 tests
Autosomal recessive limb-girdle muscular dystrophy type 2I4 tests
Autosomal recessive limb-girdle muscular dystrophy type 2J5 tests
Autosomal recessive limb-girdle muscular dystrophy type 2K3 tests
Autosomal recessive limb-girdle muscular dystrophy type 2L3 tests
Autosomal recessive limb-girdle muscular dystrophy type 2M3 tests
Autosomal recessive limb-girdle muscular dystrophy type 2N3 tests
Autosomal recessive limb-girdle muscular dystrophy type 2O3 tests
Autosomal recessive limb-girdle muscular dystrophy type 2P2 tests
Autosomal recessive limb-girdle muscular dystrophy type 2Q2 tests
Autosomal recessive limb-girdle muscular dystrophy type 2U2 tests
Autosomal recessive limb-girdle muscular dystrophy type R182 tests
Autosomal recessive nonsyndromic hearing loss 1A3 tests
Autosomal recessive nonsyndromic hearing loss 1B2 tests
Autosomal recessive spinocerebellar ataxia 103 tests
Autosomal recessive spinocerebellar ataxia 113 tests
Autosomal recessive spinocerebellar ataxia 133 tests
Autosomal recessive spinocerebellar ataxia 142 tests
Azorean disease4 tests
Bardet-Biedl syndrome4 tests
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
Becker muscular dystrophy4 tests
Bethlem myopathy 1A1 test
Bilateral frontoparietal polymicrogyria2 tests
Biotin-responsive basal ganglia disease3 tests
Borjeson-Forssman-Lehmann syndrome2 tests
Bosch-Boonstra-Schaaf optic atrophy syndrome2 tests
Brain small vessel disease 1 with or without ocular anomalies3 tests
Branched-chain keto acid dehydrogenase kinase deficiency3 tests
Brody myopathy1 test
Brugada syndrome 12 tests
Brugada syndrome 92 tests
CARASIL syndrome1 test
Carnitine palmitoyl transferase II deficiency, severe infantile form2 tests
Cataract 16 multiple types1 test
Central core myopathy1 test
Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 14 tests
Cerebral cavernous malformation2 tests
Cerebral cavernous malformation 22 tests
Cerebral cavernous malformation 32 tests
Cerebral folate transport deficiency4 tests
Ceroid lipofuscinosis, neuronal, 4 (Kufs type)2 tests
Ceroid lipofuscinosis, neuronal, 6A2 tests
Charcot-Marie-Tooth disease X-linked dominant 18 tests
Charcot-Marie-Tooth disease axonal type 2C8 tests
Charcot-Marie-Tooth disease axonal type 2F8 tests
Charcot-Marie-Tooth disease axonal type 2K9 tests
Charcot-Marie-Tooth disease axonal type 2L8 tests
Charcot-Marie-Tooth disease dominant intermediate B13 tests
Charcot-Marie-Tooth disease dominant intermediate C10 tests
Charcot-Marie-Tooth disease dominant intermediate D9 tests
Charcot-Marie-Tooth disease recessive intermediate A5 tests
Charcot-Marie-Tooth disease type 1B9 tests
Charcot-Marie-Tooth disease type 1C7 tests
Charcot-Marie-Tooth disease type 1D8 tests
Charcot-Marie-Tooth disease type 1E11 tests
Charcot-Marie-Tooth disease type 1F7 tests
Charcot-Marie-Tooth disease type 2A26 tests
Charcot-Marie-Tooth disease type 2B7 tests
Charcot-Marie-Tooth disease type 2B112 tests
Charcot-Marie-Tooth disease type 2D8 tests
Charcot-Marie-Tooth disease type 2E7 tests
Charcot-Marie-Tooth disease type 2I9 tests
Charcot-Marie-Tooth disease type 2J9 tests
Charcot-Marie-Tooth disease type 2Y1 test
Charcot-Marie-Tooth disease type 4A9 tests
Charcot-Marie-Tooth disease type 4B17 tests
Charcot-Marie-Tooth disease type 4B27 tests
Charcot-Marie-Tooth disease type 4C7 tests
Charcot-Marie-Tooth disease type 4D7 tests
Charcot-Marie-Tooth disease type 4E4 tests
Charcot-Marie-Tooth disease type 4F7 tests
Charcot-Marie-Tooth disease type 4H7 tests
Charcot-Marie-Tooth disease type 4J9 tests
Charcot-Marie-Tooth disease, axonal, with vocal cord paresis, autosomal recessive5 tests
Charcot-Marie-Tooth disease, type IA11 tests
Charlevoix-Saguenay spastic ataxia7 tests
Cholestanol storage disease2 tests
Chorea-acanthocytosis2 tests
Christianson syndrome3 tests
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency4 tests
Cleft palate, midfacial hypoplasia, triangular facies, and sensorineural hearing loss2 tests
Cohen syndrome3 tests
Complex cortical dysplasia with other brain malformations 72 tests
Compton-North congenital myopathy1 test
Congenital adrenal hypoplasia, X-linked2 tests
Congenital bile acid synthesis defect 33 tests
Congenital generalized lipodystrophy type 23 tests
Congenital generalized lipodystrophy type 41 test
Congenital lipoid adrenal hyperplasia due to STAR deficency1 test
Congenital multicore myopathy with external ophthalmoplegia1 test
Congenital muscular dystrophy due to integrin alpha-7 deficiency1 test
Congenital muscular dystrophy with intellectual disability and severe epilepsy1 test
Congenital muscular hypertrophy-cerebral syndrome2 tests
Congenital myasthenic syndrome 101 test
Congenital myasthenic syndrome 111 test
Congenital myasthenic syndrome 121 test
Congenital myasthenic syndrome 131 test
Congenital myasthenic syndrome 182 tests
Congenital myasthenic syndrome 2A1 test
Congenital myasthenic syndrome 3B1 test
Congenital myasthenic syndrome 4A1 test
Congenital myasthenic syndrome 4B1 test
Congenital myasthenic syndrome 4C1 test
Congenital myasthenic syndrome 51 test
Congenital myasthenic syndrome 81 test
Congenital myasthenic syndrome 91 test
Congenital myopathy 231 test
Congenital myopathy 4B, autosomal recessive1 test
Congenital myopathy with fiber type disproportion3 tests
Congenital myopathy with internal nuclei and atypical cores2 tests
Congenital myotonia, autosomal dominant form3 tests
Congenital myotonia, autosomal recessive form3 tests
Cornelia de Lange syndrome 12 tests
Cornelia de Lange syndrome 32 tests
Cortical dysplasia-focal epilepsy syndrome2 tests
Creatine transporter deficiency3 tests
Cutis laxa with osteodystrophy2 tests
DYRK1A-related intellectual disability syndrome2 tests
Deficiency of guanidinoacetate methyltransferase3 tests
Deficiency of steroid 11-beta-monooxygenase4 tests
Deficiency of steroid 17-alpha-monooxygenase1 test
Dentatorubral-pallidoluysian atrophy4 tests
Desmin-related myofibrillar myopathy4 tests
Developmental and epileptic encephalopathy 943 tests
Developmental and epileptic encephalopathy, 16 tests
Developmental and epileptic encephalopathy, 114 tests
Developmental and epileptic encephalopathy, 122 tests
Developmental and epileptic encephalopathy, 132 tests
Developmental and epileptic encephalopathy, 143 tests
Developmental and epileptic encephalopathy, 152 tests
Developmental and epileptic encephalopathy, 172 tests
Developmental and epileptic encephalopathy, 182 tests
Developmental and epileptic encephalopathy, 26 tests
Developmental and epileptic encephalopathy, 232 tests
Developmental and epileptic encephalopathy, 243 tests
Developmental and epileptic encephalopathy, 252 tests
Developmental and epileptic encephalopathy, 262 tests
Developmental and epileptic encephalopathy, 274 tests
Developmental and epileptic encephalopathy, 282 tests
Developmental and epileptic encephalopathy, 302 tests
Developmental and epileptic encephalopathy, 31A2 tests
Developmental and epileptic encephalopathy, 322 tests
Developmental and epileptic encephalopathy, 333 tests
Developmental and epileptic encephalopathy, 364 tests
Developmental and epileptic encephalopathy, 43 tests
Developmental and epileptic encephalopathy, 53 tests
Developmental and epileptic encephalopathy, 532 tests
Developmental and epileptic encephalopathy, 543 tests
Developmental and epileptic encephalopathy, 72 tests
Developmental and epileptic encephalopathy, 83 tests
Developmental and epileptic encephalopathy, 94 tests
DiGeorge syndrome2 tests
Diabetes insipidus, nephrogenic, X-linked2 tests
Diabetes insipidus, nephrogenic, autosomal2 tests
Diabetes mellitus, transient neonatal, 22 tests
Diabetes mellitus, transient neonatal, 32 tests
Diffuse cerebral and cerebellar atrophy - intractable seizures - progressive microcephaly syndrome3 tests
Dihydropyrimidine dehydrogenase deficiency3 tests
Dilated cardiomyopathy 1C1 test
Dilated cardiomyopathy 1II1 test
Dilated cardiomyopathy 1S1 test
Distal myopathy with posterior leg and anterior hand involvement2 tests
Duchenne muscular dystrophy4 tests
Dystonia 53 tests
Dystonia 92 tests
EAST syndrome2 tests
Early myoclonic encephalopathy3 tests
Early-onset generalized limb-onset dystonia2 tests
Early-onset myopathy with fatal cardiomyopathy4 tests
Eichsfeld type congenital muscular dystrophy3 tests
Emery-Dreifuss muscular dystrophy 2, autosomal dominant1 test
Emery-Dreifuss muscular dystrophy 4, autosomal dominant4 tests
Emery-Dreifuss muscular dystrophy 5, autosomal dominant2 tests
Emery-Dreifuss muscular dystrophy 7, autosomal dominant2 tests
Encephalopathy due to GLUT1 deficiency3 tests
Epilepsy3 tests
Epilepsy, X-linked 1, with variable learning disabilities and behavior disorders2 tests
Epilepsy, childhood absence, susceptibility to, 53 tests
Epilepsy, childhood absence, susceptibility to, 62 tests
Epilepsy, familial focal, with variable foci 12 tests
Epilepsy, familial temporal lobe, 13 tests
Epilepsy, idiopathic generalized, susceptibility to, 102 tests
Epilepsy, idiopathic generalized, susceptibility to, 132 tests
Epilepsy, idiopathic generalized, susceptibility to, 73 tests
Epilepsy, idiopathic generalized, susceptibility to, 82 tests
Epilepsy, idiopathic generalized, susceptibility to, 95 tests
Epilepsy, progressive myoclonic, 1B2 tests
Epileptic encephalopathy5 tests
Episodic ataxia type 16 tests
Episodic ataxia type 54 tests
Episodic ataxia type 64 tests
FG syndrome 41 test
Facioscapulohumeral muscular dystrophy1 test
Facioscapulohumeral muscular dystrophy 21 test
Familial X-linked hypophosphatemic vitamin D refractory rickets2 tests
Familial encephalopathy with neuroserpin inclusion bodies2 tests
Familial hypocalciuric hypercalcemia 11 test
Familial hypokalemia-hypomagnesemia2 tests
Familial infantile myasthenia1 test
Familial infantile myoclonic epilepsy2 tests
Familial isolated deficiency of vitamin E4 tests
Familial juvenile hyperuricemic nephropathy type 11 test
Familial medullary thyroid carcinoma2 tests
Familial temporal lobe epilepsy 52 tests
Fatal infantile hypertonic myofibrillar myopathy2 tests
Febrile seizures, familial, 112 tests
Febrile seizures, familial, 42 tests
Febrile seizures, familial, 83 tests
Finnish congenital nephrotic syndrome2 tests
Focal epilepsy2 tests
Focal segmental glomerulosclerosis 12 tests
Focal segmental glomerulosclerosis 22 tests
Focal segmental glomerulosclerosis 52 tests
Friedreich ataxia 15 tests
Frontotemporal dementia2 tests
Frontotemporal dementia and/or amyotrophic lateral sclerosis 14 tests
Frontotemporal dementia and/or amyotrophic lateral sclerosis 32 tests
Frontotemporal dementia and/or amyotrophic lateral sclerosis 62 tests
Frontotemporal dementia and/or amyotrophic lateral sclerosis 72 tests
GM3 synthase deficiency3 tests
GNE myopathy1 test
GRN-related frontotemporal lobar degeneration with Tdp43 inclusions2 tests
Gamma-aminobutyric acid transaminase deficiency3 tests
Generalized epilepsy with febrile seizures plus, type 13 tests
Generalized epilepsy with febrile seizures plus, type 25 tests
Generalized epilepsy with febrile seizures plus, type 72 tests
Generalized epilepsy with febrile seizures plus, type 92 tests
Gillespie syndrome3 tests
Glaucoma, normal tension, susceptibility to1 test
Glucocorticoid-remediable aldosteronism1 test
Goldberg-Shprintzen syndrome2 tests
Gonadotropin-independent familial sexual precocity1 test
HSD10 mitochondrial disease2 tests
Hereditary disease1 test
Hereditary insensitivity to pain with anhidrosis2 tests
Hereditary sensory and autonomic neuropathy type 12 tests
Hereditary spastic paraplegia 104 tests
Hereditary spastic paraplegia 115 tests
Hereditary spastic paraplegia 124 tests
Hereditary spastic paraplegia 134 tests
Hereditary spastic paraplegia 155 tests
Hereditary spastic paraplegia 174 tests
Hereditary spastic paraplegia 23 tests
Hereditary spastic paraplegia 304 tests
Hereditary spastic paraplegia 314 tests
Hereditary spastic paraplegia 354 tests
Hereditary spastic paraplegia 394 tests
Hereditary spastic paraplegia 3A5 tests
Hereditary spastic paraplegia 45 tests
Hereditary spastic paraplegia 424 tests
Hereditary spastic paraplegia 484 tests
Hereditary spastic paraplegia 5A4 tests
Hereditary spastic paraplegia 64 tests
Hereditary spastic paraplegia 75 tests
Hereditary spastic paraplegia 84 tests
Heterotopia, periventricular, X-linked dominant2 tests
Holoprosencephaly 22 tests
Holoprosencephaly 32 tests
Huntington disease2 tests
Huppke-Brendel syndrome3 tests
Hyperinsulinemic hypoglycemia, familial, 12 tests
Hyperinsulinemic hypoglycemia, familial, 22 tests
Hyperinsulinism due to glucokinase deficiency2 tests
Hyperinsulinism-hyperammonemia syndrome2 tests
Hyperphosphatasia with intellectual disability syndrome 12 tests
Hyperphosphatasia with intellectual disability syndrome 22 tests
Hypertrophic cardiomyopathy 11 test
Hypogonadotropic hypogonadism 1 with or without anosmia3 tests
Hypogonadotropic hypogonadism 11 with or without anosmia3 tests
Hypogonadotropic hypogonadism 12 with or without anosmia3 tests
Hypogonadotropic hypogonadism 2 with or without anosmia4 tests
Hypogonadotropic hypogonadism 3 with or without anosmia4 tests
Hypogonadotropic hypogonadism 4 with or without anosmia4 tests
Hypogonadotropic hypogonadism 5 with or without anosmia2 tests
Hypogonadotropic hypogonadism 6 with or without anosmia3 tests
Hypogonadotropic hypogonadism 7 with or without anosmia4 tests
Hypogonadotropic hypogonadism 8 with or without anosmia4 tests
Hypokalemic periodic paralysis, type 11 test
Hypokalemic periodic paralysis, type 24 tests
Hypomyelinating leukodystrophy 21 test
Hypomyelinating leukodystrophy 43 tests
Idiopathic generalized epilepsy1 test
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 12 tests
Infantile hypophosphatasia2 tests
Infantile neuroaxonal dystrophy2 tests
Infantile onset spinocerebellar ataxia2 tests
Infantile spasms2 tests
Infantile-onset X-linked spinal muscular atrophy2 tests
Intellectual disability, X-linked 12 tests
Intellectual disability, X-linked 302 tests
Intellectual disability, X-linked 722 tests
Intellectual disability, X-linked 962 tests
Intellectual disability, X-linked, with or without seizures, arx-related2 tests
Intellectual disability, autosomal dominant 12 tests
Intellectual disability, autosomal dominant 203 tests
Intellectual disability, autosomal dominant 243 tests
Intellectual disability, autosomal dominant 54 tests
Intellectual disability, autosomal dominant 82 tests
Intellectual disability, autosomal dominant 93 tests
Intellectual disability-epilepsy-extrapyramidal syndrome3 tests
Intellectual disability-hypotonic facies syndrome, X-linked, 12 tests
Isolated focal cortical dysplasia type II4 tests
Isolated growth hormone deficiency type IB3 tests
Joubert syndrome 22 tests
Joubert syndrome 32 tests
Joubert syndrome 52 tests
Joubert syndrome 62 tests
Joubert syndrome 92 tests
Joubert syndrome with renal defect2 tests
KBG syndrome2 tests
Kabuki syndrome 11 test
Kennedy disease1 test
Keratosis follicularis2 tests
Koolen-de Vries syndrome2 tests
Kufor-Rakeb syndrome2 tests
Kugelberg-Welander disease4 tests
L-2-hydroxyglutaric aciduria2 tests
LAMB2-related infantile-onset nephrotic syndrome2 tests
Lafora disease2 tests
Landau-Kleffner syndrome4 tests
Laurence-Moon syndrome3 tests
Lesch-Nyhan syndrome2 tests
Leucine-induced hypoglycemia2 tests
Liddle syndrome 15 tests
Lipoic acid synthetase deficiency3 tests
Lissencephaly 42 tests
Lissencephaly due to LIS1 mutation2 tests
Lissencephaly due to TUBA1A mutation2 tests
Lissencephaly type 1 due to doublecortin gene mutation3 tests
Long QT syndrome 22 tests
Luscan-Lumish syndrome2 tests
MASA syndrome3 tests
MEGF10-related myopathy1 test
MYH7-related skeletal myopathy1 test
Macrocephaly-autism syndrome1 test
Malignant hyperthermia, susceptibility to, 11 test
Malignant hyperthermia, susceptibility to, 51 test
Marinesco-Sjögren syndrome3 tests
Mast syndrome4 tests
Maturity-onset diabetes of the young type 13 tests
Maturity-onset diabetes of the young type 25 tests
Maturity-onset diabetes of the young type 35 tests
Maturity-onset diabetes of the young type 42 tests
Maturity-onset diabetes of the young type 81 test
Megaconial type congenital muscular dystrophy1 test
Merosin deficient congenital muscular dystrophy3 tests
Metachromatic leukodystrophy1 test
Microcephaly 1, primary, autosomal recessive4 tests
Microcephaly 2, primary, autosomal recessive, with or without cortical malformations4 tests
Microcephaly 5, primary, autosomal recessive5 tests
Microcephaly 6, primary, autosomal recessive2 tests
Microcephaly 7, primary, autosomal recessive2 tests
Microcephaly, seizures, and developmental delay2 tests
Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome2 tests
Migraine, familial hemiplegic, 19 tests
Migraine, familial hemiplegic, 24 tests
Migraine, familial hemiplegic, 34 tests
Mitochondrial DNA depletion syndrome 11 test
Mitochondrial DNA depletion syndrome 12B (cardiomyopathic type), autosomal recessive1 test
Mitochondrial DNA depletion syndrome 3 (hepatocerebral type)2 tests
Mitochondrial DNA depletion syndrome 4b3 tests
Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)2 tests
Mitochondrial DNA depletion syndrome 8a2 tests
Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria2 tests
Mitochondrial DNA depletion syndrome, myopathic form2 tests
Mitochondrial complex I deficiency2 tests
Miyoshi muscular dystrophy 13 tests
Miyoshi muscular dystrophy 32 tests
Mowat-Wilson syndrome2 tests
Multiple congenital anomalies-hypotonia-seizures syndrome 13 tests
Multiple congenital anomalies-hypotonia-seizures syndrome 23 tests
Multiple endocrine neoplasia type 2A2 tests
Multiple endocrine neoplasia type 2B2 tests
Multiple endocrine neoplasia, type 11 test
Muscle eye brain disease4 tests
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 44 tests
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 72 tests
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A14 tests
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A131 test
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A24 tests
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A56 tests
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A63 tests
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A91 test
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 101 test
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 111 test
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 81 test
Muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B12 tests
Muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B22 tests
Muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B32 tests
Muscular dystrophy-dystroglycanopathy (congenital without intellectual disability), type B42 tests
Muscular dystrophy-dystroglycanopathy type B54 tests
Muscular dystrophy-dystroglycanopathy type B61 test
Myasthenic syndrome, congenital, 1B, fast-channel1 test
Myasthenic syndrome, slow-channel congenital1 test
Myoclonic dystonia 112 tests
Myoclonic-astatic epilepsy2 tests
Myofibrillar myopathy 22 tests
Myofibrillar myopathy 34 tests
Myofibrillar myopathy 42 tests
Myofibrillar myopathy 52 tests
Myofibrillar myopathy 61 test
Myopathy, centronuclear, 21 test
Myopathy, myofibrillar, 9, with early respiratory failure4 tests
Myopathy, myosin storage, autosomal recessive2 tests
Myopathy, proximal, and ophthalmoplegia1 test
Myopathy, reducing body, X-linked, childhood-onset3 tests
Myopathy, reducing body, X-linked, early-onset, severe3 tests
Myosin storage myopathy2 tests
Myotonic dystrophy type 22 tests
NDE1-related microhydranencephaly2 tests
Nemaline myopathy 22 tests
Nemaline myopathy 51 test
Nemaline myopathy 61 test
Nemaline myopathy 71 test
Nemaline myopathy 81 test
Neonatal-onset encephalopathy with rigidity and seizures3 tests
Nephronophthisis 11 test
Nephrotic syndrome 152 tests
Nephrotic syndrome, type 23 tests
Nephrotic syndrome, type 32 tests
Nephrotic syndrome, type 42 tests
Neurodegeneration with brain iron accumulation 53 tests
Neurofibromatosis, type 13 tests
Neurofibromatosis, type 23 tests
Neuronal ceroid lipofuscinosis 12 tests
Neuronal ceroid lipofuscinosis 102 tests
Neuronal ceroid lipofuscinosis 112 tests
Neuronal ceroid lipofuscinosis 132 tests
Neuronal ceroid lipofuscinosis 22 tests
Neuronal ceroid lipofuscinosis 32 tests
Neuronal ceroid lipofuscinosis 52 tests
Neuronal ceroid lipofuscinosis 72 tests
Neuronal ceroid lipofuscinosis 82 tests
Neuronopathy, distal hereditary motor, type 2C1 test
Neuronopathy, distal hereditary motor, type 5A3 tests
Neuronopathy, distal hereditary motor, type 5B3 tests
Neuronopathy, distal hereditary motor, type 7B1 test
Neuropathy, hereditary sensory and autonomic, type 1C2 tests
Neuropathy, hereditary sensory and autonomic, type 2A2 tests
Neuropathy, hereditary sensory, type 1D1 test
Neuropathy, hereditary sensory, type 2C3 tests
Non-ketotic hyperglycinemia3 tests
Noonan syndrome 11 test
Noonan syndrome 32 tests
Noonan syndrome 42 tests
Noonan syndrome 52 tests
Norman-Roberts syndrome2 tests
Obesity2 tests
Obesity due to leptin receptor gene deficiency2 tests
Oculopharyngeal muscular dystrophy1 test
Optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy2 tests
Orofaciodigital syndrome I2 tests
Osteogenesis imperfecta type I2 tests
Osteogenesis imperfecta type III3 tests
Osteogenesis imperfecta with normal sclerae, dominant form3 tests
Osteogenesis imperfecta, perinatal lethal3 tests
Osteoporosis with pseudoglioma1 test
PHGDH deficiency2 tests
PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome3 tests
Paget disease of bone 31 test
Paroxysmal nonkinesigenic dyskinesia 11 test
Partington syndrome2 tests
Pelger-Huët anomaly2 tests
Pelizaeus-Merzbacher disease5 tests
Periventricular heterotopia with microcephaly, autosomal recessive2 tests
Permanent neonatal diabetes mellitus7 tests
Peroxisome biogenesis disorder 9B2 tests
Perry syndrome1 test
Phelan-McDermid syndrome1 test
Pheochromocytoma3 tests
Pierpont syndrome2 tests
Pigmentary pallidal degeneration2 tests
Pitt-Hopkins syndrome2 tests
Pitt-Hopkins-like syndrome 22 tests
Pituitary hormone deficiency, combined, 12 tests
Pituitary hormone deficiency, combined, 22 tests
Polycystic kidney disease 25 tests
Polycystic kidney disease, adult type5 tests
Polyglandular autoimmune syndrome, type 12 tests
Polymicrogyria with optic nerve hypoplasia2 tests
Pontocerebellar hypoplasia type 1A1 test
Pontocerebellar hypoplasia type 2A2 tests
Pontocerebellar hypoplasia type 42 tests
Posterior column ataxia-retinitis pigmentosa syndrome3 tests
Postmenopausal osteoporosis1 test
Potassium-aggravated myotonia5 tests
Primary open angle glaucoma1 test
Progressive demyelinating neuropathy with bilateral striatal necrosis4 tests
Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 13 tests
Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 21 test
Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 32 tests
Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 52 tests
Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 13 tests
Progressive myoclonic epilepsy type 33 tests
Progressive myoclonic epilepsy type 62 tests
Progressive myoclonic epilepsy type 72 tests
Progressive myoclonic epilepsy type 92 tests
Progressive sclerosing poliodystrophy4 tests
Pseudohypoaldosteronism, type IB1, autosomal recessive6 tests
Pyridoxal phosphate-responsive seizures3 tests
Pyridoxine-dependent epilepsy2 tests
Pyruvate dehydrogenase complex deficiency1 test
Renal cysts and diabetes syndrome4 tests
Renpenning syndrome3 tests
Rett syndrome2 tests
Rett syndrome, congenital variant4 tests
Rippling muscle disease 25 tests
Ritscher-Schinzel syndrome 13 tests
Rolandic epilepsy, intellectual disability, and speech dyspraxia, X-linked3 tests
SHOX-related short stature2 tests
SLC35A2-congenital disorder of glycosylation5 tests
Sarcotubular myopathy3 tests
Schinzel-Giedion syndrome2 tests
Schizencephaly2 tests
Schwannomatosis 13 tests
Schwartz-Jampel syndrome1 test
Seizure2 tests
Seizures, benign familial infantile, 24 tests
Seizures, benign familial neonatal, 22 tests
Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis10 tests
Severe X-linked myotubular myopathy1 test
Severe myoclonic epilepsy in infancy2 tests
Severe neonatal-onset encephalopathy with microcephaly4 tests
Severe neurodegenerative syndrome with lipodystrophy3 tests
Short stature due to partial GHR deficiency1 test
Simpson-Golabi-Behmel syndrome type 12 tests
Sleep-related hypermotor epilepsy2 tests
Smith-Lemli-Opitz syndrome1 test
Smith-Magenis syndrome2 tests
Spastic ataxia 13 tests
Spastic ataxia 43 tests
Spastic ataxia 54 tests
Spinal muscular atrophy, type II4 tests
Spinal muscular atrophy, type IV4 tests
Spinal muscular atrophy-progressive myoclonic epilepsy syndrome2 tests
Spinocerebellar ataxia 74 tests
Spinocerebellar ataxia type 14 tests
Spinocerebellar ataxia type 104 tests
Spinocerebellar ataxia type 113 tests
Spinocerebellar ataxia type 123 tests
Spinocerebellar ataxia type 133 tests
Spinocerebellar ataxia type 143 tests
Spinocerebellar ataxia type 15/163 tests
Spinocerebellar ataxia type 174 tests
Spinocerebellar ataxia type 19/223 tests
Spinocerebellar ataxia type 24 tests
Spinocerebellar ataxia type 233 tests
Spinocerebellar ataxia type 263 tests
Spinocerebellar ataxia type 273 tests
Spinocerebellar ataxia type 285 tests
Spinocerebellar ataxia type 293 tests
Spinocerebellar ataxia type 353 tests
Spinocerebellar ataxia type 53 tests
Spinocerebellar ataxia type 61 test
Spinocerebellar ataxia type 84 tests
Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 13 tests
Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 25 tests
Steinert myotonic dystrophy syndrome3 tests
Syndromic X-linked intellectual disability 942 tests
Syndromic X-linked intellectual disability Claes-Jensen type2 tests
Syndromic X-linked intellectual disability Hedera type2 tests
Syndromic X-linked intellectual disability Snyder type2 tests
Tibial muscular dystrophy4 tests
Torsion dystonia 62 tests
Tremor, hereditary essential, 41 test
Trichomegaly-retina pigmentary degeneration-dwarfism syndrome3 tests
Troyer syndrome4 tests
Tuberous sclerosis 13 tests
Tuberous sclerosis 27 tests
Type 2 diabetes mellitus7 tests
Ullrich congenital muscular dystrophy 1A1 test
Unverricht-Lundborg syndrome2 tests
Vanishing white matter disease6 tests
Von Hippel-Lindau syndrome2 tests
Warburg micro syndrome 12 tests
Welander distal myopathy1 test
Werdnig-Hoffmann disease4 tests
West syndrome2 tests
X-linked Alport syndrome3 tests
X-linked Emery-Dreifuss muscular dystrophy2 tests
X-linked complicated corpus callosum dysgenesis3 tests
X-linked hydrocephalus syndrome3 tests
X-linked intellectual disability Cabezas type2 tests
X-linked intellectual disability, Cantagrel type2 tests
X-linked intellectual disability-cerebellar hypoplasia syndrome2 tests
X-linked lissencephaly with abnormal genitalia3 tests
X-linked myopathy with postural muscle atrophy4 tests