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Clinical Genomics Laboratory (Washington University in St. Louis)

General information

Clinical Genomics Laboratory
Washington University in St. Louis
4320 Forest Park Avenue
CORTEX building, Suite 207
St.Louis
Missouri
United States - 63108
http://gps.wustl.edu/
Organization ID: 505219

Personnel

View this laboratory in GTR

Assertion criteria

Level: Assertion criteria provided

Summary of submissions to ClinVar

Total submissions: 700

Gene

GeneSubmissionsLast Updated
ABCA121May 22, 2024
ABCC81May 22, 2024
ABL11Dec 12, 2023
ABTB31Dec 12, 2023
ACADSB1May 21, 2024
ACBD61May 21, 2024
ACSS21May 21, 2024
ACVRL11Dec 12, 2023
ADA21Dec 12, 2023
ADAMTS102May 21, 2024
ADAMTS134May 22, 2024
ADAMTS191May 21, 2024
ADCY51May 21, 2024
ADCY62May 21, 2024
ADGRB11May 21, 2024
ADGRL12May 21, 2024
ADGRL1-AS11May 21, 2024
AIRE2May 22, 2024
AKT11Dec 12, 2023
ANK21Dec 12, 2023
ANKRD112May 21, 2024
ANLN1May 22, 2024
APOL12Dec 12, 2023
ARAF2Dec 12, 2023
ARFGEF11May 21, 2024
ARHGEF121May 21, 2024
ASH1L1May 21, 2024
ASIC21May 21, 2024
ASXL31May 21, 2024
ATG4D1May 21, 2024
ATP11A1May 21, 2024
ATP1A31Dec 12, 2023
ATP6V1B21Dec 12, 2023
ATRX1Dec 12, 2023
BAZ2B1Dec 12, 2023
BCL11A1Dec 12, 2023
BMP8B1May 21, 2024
BNC21Dec 12, 2023
BRAF2May 22, 2024
BRCA11May 21, 2024
BRCA22May 21, 2024
BRPF12May 21, 2024
BSN2May 21, 2024
CACNA1A3May 21, 2024
CACNA1C1May 21, 2024
CACNA1D1May 21, 2024
CACNA1E1May 21, 2024
CACNA1F1May 21, 2024
CARD141Dec 12, 2023
CBS1May 21, 2024
CCBE12May 22, 2024
CCDST4May 21, 2024
CCM21May 22, 2024
CCND21May 22, 2024
CCNH7May 22, 2024
CDC421Dec 12, 2023
CDC42BPB1Dec 12, 2023
CDK131Dec 12, 2023
CDKN1C1Dec 12, 2023
CEL1May 22, 2024
CELSR111May 22, 2024
CFAP741May 21, 2024
CFH2May 22, 2024
CFHR41May 22, 2024
CFHR51May 22, 2024
CFTR1May 21, 2024
CHD11Dec 12, 2023
CHD21Dec 12, 2023
CHD31Dec 12, 2023
CHD52May 21, 2024
CHD71Dec 12, 2023
CLDN142Dec 12, 2023
CLDN14-AS12Dec 12, 2023
COG11May 21, 2024
COL10A11Dec 12, 2023
COL11A11May 21, 2024
COL11A21Dec 12, 2023
COL1A11May 21, 2024
COL21A12May 21, 2024
COL22A12May 21, 2024
COL4A32May 22, 2024
COL4A51May 22, 2024
COL9A21Dec 12, 2023
CPEB41Dec 12, 2023
CPOX1Dec 12, 2023
CPT21May 21, 2024
CREBBP1May 21, 2024
CSTB1May 21, 2024
CTNNB13May 22, 2024
CUBN3May 22, 2024
CYP51A12May 21, 2024
DAGLA1Dec 12, 2023
DCHS111May 22, 2024
DEAF11Dec 12, 2023
DEPDC51May 21, 2024
DGKE1Dec 12, 2023
DHTKD11Dec 12, 2023
DLG42May 21, 2024
DLL12May 21, 2024
DMD1May 21, 2024
DMXL22Dec 12, 2023
DNAH111Dec 12, 2023
DNAH52Dec 12, 2023
DNAH81Dec 12, 2023
DNASE11May 21, 2024
DPYD1May 21, 2024
DPYSL21May 21, 2024
DPYSL31Dec 12, 2023
DRD41May 21, 2024
DSG21May 21, 2024
DSG2-AS11May 21, 2024
DSP1Dec 12, 2023
DUSP151May 21, 2024
DVL11Dec 12, 2023
DYNC1H11May 21, 2024
EARS21Dec 12, 2023
EEF1A11Dec 12, 2023
EFTUD21May 21, 2024
EIF3F1Dec 12, 2023
EMP22May 22, 2024
EPHB48May 22, 2024
ERCC41May 21, 2024
ESCO21May 21, 2024
EXT11Dec 12, 2023
EYA11Dec 12, 2023
F111May 21, 2024
FAT11May 22, 2024
FAT418May 22, 2024
FBN31May 21, 2024
FBXW111Dec 12, 2023
FFAR41May 21, 2024
FGFR13May 22, 2024
FGFR23May 22, 2024
FGFR31Dec 12, 2023
FHOD31May 21, 2024
FLG4May 21, 2024
FLNA1May 21, 2024
FLNC1May 21, 2024
FLT44May 22, 2024
FRMD71Dec 12, 2023
GABBR11May 21, 2024
GABBR21Dec 12, 2023
GATAD11May 21, 2024
GBA11May 21, 2024
GBF11May 21, 2024
GCK1May 22, 2024
GFAP1May 21, 2024
GH-LCR1Dec 12, 2023
GJA41May 22, 2024
GJC22Dec 12, 2023
GLI21May 21, 2024
GLMN6May 22, 2024
GNA112May 22, 2024
GNA142Dec 12, 2023
GNAQ4May 22, 2024
GNAS9May 22, 2024
GNAS-AS11May 22, 2024
GPD21May 21, 2024
GRIA11Dec 12, 2023
HCFC11Dec 12, 2023
HDAC41May 21, 2024
HECW21Dec 12, 2023
HERC11May 21, 2024
HFE1Dec 12, 2023
HGF1May 22, 2024
HNF1A1May 22, 2024
HNF4A1Dec 12, 2023
HNRNPU1Dec 12, 2023
HOMER21May 21, 2024
HRAS6May 22, 2024
HSALR12May 22, 2024
HUWE13May 21, 2024
IDH12May 22, 2024
IDH22May 22, 2024
IDUA1May 21, 2024
IFIH11May 21, 2024
IL71Dec 12, 2023
IMMT1May 21, 2024
INTS111May 21, 2024
INVS1Dec 12, 2023
IQSEC22Dec 12, 2023
ITPR11May 21, 2024
ITSN11Dec 12, 2023
JARID21May 21, 2024
JMJD1C1Dec 12, 2023
KANK11May 22, 2024
KAT52May 21, 2024
KCNC11May 21, 2024
KCNH23Dec 12, 2023
KCNQ12Dec 12, 2023
KCNQ51Dec 12, 2023
KDM3B1May 21, 2024
KDM5B1May 21, 2024
KDR3May 22, 2024
KEL3May 22, 2024
KIDINS2201Dec 12, 2023
KIF111Dec 12, 2023
KIF1A1Dec 12, 2023
KIF21A1May 21, 2024
KIF5A1Dec 12, 2023
KLF9-DT1May 21, 2024
KMT2A2Dec 12, 2023
KMT2B2May 21, 2024
KMT2D2May 21, 2024
KMT2E1Dec 12, 2023
KRAS4May 22, 2024
KRIT14May 22, 2024
KRT12Dec 12, 2023
KRT102May 22, 2024
KRT10-AS12May 22, 2024
LDLR1May 21, 2024
LHX41May 21, 2024
LHX4-AS11May 21, 2024
LIPE1May 21, 2024
LIPE-AS11May 21, 2024
LMNA1May 22, 2024
LOC1019300711May 21, 2024
LOC1027240582Dec 12, 2023
LOC1066279811May 21, 2024
LOC1216279521Dec 12, 2023
LOC1268066582May 22, 2024
LOC1268066591Dec 12, 2023
LOC1268068781May 21, 2024
LOC1268601242Dec 12, 2023
LOC1268605541May 22, 2024
LOC1268605851Dec 12, 2023
LOC1268618871Dec 12, 2023
LOC1268630181May 21, 2024
LOC1293901431May 22, 2024
LOC1299304461May 21, 2024
LOC1299993031Dec 12, 2023
LOC1300043401May 21, 2024
LOC1300584791May 21, 2024
LOC1300664201May 22, 2024
LOC1300668131Dec 12, 2023
LPL1May 21, 2024
LRP21May 21, 2024
LRRC566May 22, 2024
LRRK21May 21, 2024
LRSAM11May 21, 2024
LZTR110May 22, 2024
MAGEL21Dec 12, 2023
MAP1B1Dec 12, 2023
MAP2K15May 22, 2024
MAP3K31Dec 12, 2023
MAPK8IP31Dec 12, 2023
MARK21Dec 12, 2023
MAST21May 21, 2024
MC4R1May 21, 2024
MED133Dec 12, 2023
MED13L1Dec 12, 2023
MET2May 22, 2024
MFF-DT2May 22, 2024
MID11May 21, 2024
MMACHC1May 21, 2024
MSH22May 21, 2024
MSH62May 21, 2024
MSI21Dec 12, 2023
MTOR8May 22, 2024
MXRA51Dec 12, 2023
MYBPC34May 22, 2024
MYCN1Dec 12, 2023
MYH31May 21, 2024
MYH72May 22, 2024
MYO101Dec 12, 2023
NAA101May 21, 2024
NAA151May 21, 2024
NAGLU1May 21, 2024
NALCN1May 21, 2024
NCOR11Dec 12, 2023
NDUFA91Dec 12, 2023
NEBL1May 22, 2024
NEDD4L2Dec 12, 2023
NEXMIF1May 21, 2024
NF18May 22, 2024
NLRP31May 21, 2024
NMNAT11May 21, 2024
NPR21May 21, 2024
NRAS2Dec 12, 2023
NRXN31May 21, 2024
NSD11May 21, 2024
NT5DC11Dec 12, 2023
NUP2051May 22, 2024
NYX1May 21, 2024
OBSCN1May 22, 2024
OCA22Dec 12, 2023
PACS11Dec 12, 2023
PALB23May 21, 2024
PCGF21Dec 12, 2023
PDE11A1Dec 12, 2023
PDE4D1May 21, 2024
PDGFRB3May 22, 2024
PEX11May 21, 2024
PHF141Dec 12, 2023
PHIP1May 21, 2024
PIDD12May 21, 2024
PIEZO121May 22, 2024
PIK3CA28May 22, 2024
PIK3CD2May 22, 2024
PIK3R13May 22, 2024
PIK3R21Dec 12, 2023
PKD12May 22, 2024
PKP21May 22, 2024
PLCE11May 22, 2024
PLCG21May 21, 2024
PLEC1Dec 12, 2023
PLP11May 21, 2024
PLXNA31Dec 12, 2023
PMM21May 22, 2024
PMP21May 21, 2024
PMS22May 21, 2024
PNPLA31Oct 18, 2024
POGLUT11May 21, 2024
POGZ2May 21, 2024
POLD11May 21, 2024
POLR2A3May 21, 2024
POLRMT2May 21, 2024
POT11May 21, 2024
PPFIA31Dec 12, 2023
PPP1R3F1May 21, 2024
PPP2R5D1May 21, 2024
PRICKLE22May 21, 2024
PRICKLE2-AS12May 21, 2024
PRKACA2May 22, 2024
PSMB111Dec 12, 2023
PTEN3May 22, 2024
PTPN111Dec 12, 2023
PTPN148May 22, 2024
RAB5A1Dec 12, 2023
RAB9B1May 21, 2024
RANBP21Dec 12, 2023
RASA18May 22, 2024
RELN1Dec 12, 2023
RERE1Dec 12, 2023
RET1Dec 12, 2023
REV3L1Dec 12, 2023
RHEB1May 22, 2024
RNASEH2B1May 21, 2024
ROBO41May 21, 2024
ROR21May 21, 2024
RORA1Dec 12, 2023
RORA-AS11Dec 12, 2023
RRAS1Dec 12, 2023
RYR11May 21, 2024
SALL11May 21, 2024
SCN1A2Dec 12, 2023
SCN2A1Dec 12, 2023
SCN4A1Dec 12, 2023
SCN5A1Dec 12, 2023
SCN8A1May 21, 2024
SDHA1Dec 12, 2023
SEMA6D1Dec 12, 2023
SERPINA11Dec 12, 2023
SH3RF21May 21, 2024
SHANK11Dec 12, 2023
SHANK31Dec 12, 2023
SHOC22May 22, 2024
SIK11Dec 12, 2023
SLC12A21Dec 12, 2023
SLC17A81Dec 12, 2023
SLC1A21Dec 12, 2023
SLC25A462Dec 12, 2023
SLC35F11Dec 12, 2023
SLITRK21May 21, 2024
SMAD31Dec 12, 2023
SMO9May 22, 2024
SNAPC42Dec 12, 2023
SOCS11May 21, 2024
SON1May 21, 2024
SOS11May 22, 2024
SOS21May 21, 2024
SOX181May 22, 2024
SPG111May 21, 2024
SPI11Dec 12, 2023
SPOP1May 21, 2024
SPTAN11May 21, 2024
SPTBN12May 21, 2024
STAG21May 21, 2024
STAT5B1Dec 12, 2023
STX81Dec 12, 2023
SUPT16H1Dec 12, 2023
SYNGAP12Dec 12, 2023
SYNGAP1-AS12Dec 12, 2023
SYP1Dec 12, 2023
SYP-AS11Dec 12, 2023
TAOK11May 21, 2024
TBL1XR11May 21, 2024
TBL1XR1-AS11May 21, 2024
TBX51May 21, 2024
TEK16May 22, 2024
TET33May 21, 2024
TGFBR11May 21, 2024
THBD2May 22, 2024
THSD11May 21, 2024
TIE11May 21, 2024
TINF21May 21, 2024
TJP11May 22, 2024
TLK21May 21, 2024
TMC11May 21, 2024
TNKS21May 21, 2024
TNRC6B2Dec 12, 2023
TOP2B1May 21, 2024
TP531Aug 21, 2017
TP631Dec 12, 2023
TRIM631May 22, 2024
TRIP121Dec 12, 2023
TRPM31May 21, 2024
TRRAP2May 21, 2024
TSC16May 22, 2024
TSC25May 22, 2024
TTN11Jul 1, 2024
TTN-AS19Jul 1, 2024
TTR1May 21, 2024
TUBB31May 21, 2024
UBA21Dec 12, 2023
UBXN71Dec 12, 2023
UCP31May 21, 2024
UPF21Dec 12, 2023
VAX21Dec 12, 2023
VCF11May 21, 2024
WBP111May 21, 2024
WDFY32May 21, 2024
WDR112Dec 12, 2023
WDR242Dec 12, 2023
WFS11May 22, 2024
WNT10A1May 21, 2024
WWP11Dec 12, 2023
ZBTB201Dec 12, 2023
ZC2HC1A1Dec 12, 2023
ZFHX31May 21, 2024
ZFHX41May 21, 2024
ZNF4621Dec 12, 2023
ZNF4691May 21, 2024
ZNF8271Dec 12, 2023
ZNF8651May 21, 2024

Condition

NameSubmissionsLast Updated
13q12.3 microdeletion1Jan 7, 2020
2-aminoadipic 2-oxoadipic aciduria1Dec 12, 2023
ACCES syndrome1Dec 12, 2023
APOL1-associated kidney disease2Dec 12, 2023
ARAF-related disorder1Dec 12, 2023
Acrocephalosyndactyly type I1May 22, 2024
Acrodysostosis 2 with or without hormone resistance1May 21, 2024
Agammaglobulinemia 10, autosomal dominant1Dec 12, 2023
Aicardi-Goutieres syndrome 21May 21, 2024
Aldosterone-producing adenoma with seizures and neurological abnormalities1May 21, 2024
Alexander disease1May 21, 2024
Alpha thalassemia-X-linked intellectual disability syndrome1Dec 12, 2023
Alpha-1-antitrypsin deficiency1Dec 12, 2023
Alport syndrome 3b, autosomal recessive1May 22, 2024
Alternating hemiplegia of childhood 21Dec 12, 2023
Amyloidosis, hereditary systemic 11May 21, 2024
Ankyloblepharon filiforme adnatum-cleft palate syndrome1Dec 12, 2023
Aortic valve disease 31May 21, 2024
Arrhythmogenic right ventricular dysplasia 101May 21, 2024
Arrhythmogenic right ventricular dysplasia 81Dec 12, 2023
Arrhythmogenic right ventricular dysplasia 91May 22, 2024
Atypical hemolytic-uremic syndrome with thrombomodulin anomaly2May 22, 2024
Autism3Dec 12, 2023
Autoinflammation-PLCG2-associated antibody deficiency-immune dysregulation1May 21, 2024
Autoinflammatory syndrome with immunodeficiency1May 21, 2024
Autosomal dominant Alport syndrome1Dec 12, 2023
Autosomal dominant Parkinson disease 81May 21, 2024
Autosomal dominant Robinow syndrome 21Dec 12, 2023
Autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures1May 21, 2024
Autosomal dominant deafness - onychodystrophy syndrome1Dec 12, 2023
Autosomal dominant nonsyndromic hearing loss 251Dec 12, 2023
Autosomal dominant nonsyndromic hearing loss 681May 21, 2024
Autosomal dominant polycystic kidney disease1Dec 12, 2023
Autosomal recessive Alport syndrome1Dec 12, 2023
Autosomal recessive Robinow syndrome1May 21, 2024
Autosomal recessive congenital ichthyosis 4B1May 22, 2024
Autosomal recessive limb-girdle muscular dystrophy type 2J2Dec 12, 2023
Autosomal recessive limb-girdle muscular dystrophy type 2Q1Dec 12, 2023
Autosomal recessive limb-girdle muscular dystrophy type 2R11May 21, 2024
Autosomal recessive nonsyndromic hearing loss 391May 22, 2024
Autosomal recessive nonsyndromic hearing loss 71May 21, 2024
B-cell immunodeficiency, distal limb anomalies, and urogenital malformations1May 21, 2024
BAZ2B-associated neurodevelopmental disorder1Dec 12, 2023
Beck-Fahrner syndrome3May 21, 2024
Becker muscular dystrophy1May 21, 2024
Beckwith-Wiedemann syndrome1Dec 12, 2023
Body mass index quantitative trait locus 101May 21, 2024
Branchiootorenal syndrome 11Dec 12, 2023
Breast-ovarian cancer, familial, susceptibility to, 11May 21, 2024
Breast-ovarian cancer, familial, susceptibility to, 22May 21, 2024
Breast-ovarian cancer, familial, susceptibility to, 51May 21, 2024
Brittle cornea syndrome 11May 21, 2024
Brugada syndrome 11Dec 12, 2023
CFHR5 deficiency1May 22, 2024
CHARGE syndrome1Dec 12, 2023
COG1 congenital disorder of glycosylation1May 21, 2024
Capillary infantile hemangioma2May 22, 2024
Capillary malformation2Dec 12, 2023
Capillary malformation-arteriovenous malformation 16May 22, 2024
Capillary malformation-arteriovenous malformation 23May 22, 2024
Carcinoma of colon1Aug 21, 2017
Cardiac anomalies - developmental delay - facial dysmorphism syndrome1Dec 12, 2023
Cardiac valvular dysplasia 21May 21, 2024
Cardioacrofacial dysplasia 12May 22, 2024
Cardiofaciocutaneous syndrome 32May 22, 2024
Cardiomyopathy, familial hypertrophic, 281May 21, 2024
Carnitine palmitoyl transferase II deficiency, myopathic form1May 21, 2024
Cerebral arteriovenous malformation1Dec 12, 2023
Cerebral cavernous malformation3May 22, 2024
Cerebral cavernous malformation 21May 22, 2024
Charcot-Marie-Tooth Disease, axonal, type 2GG1May 21, 2024
Charcot-Marie-Tooth disease axonal type 2P1May 21, 2024
Charcot-Marie-Tooth disease, demyelinating, type 1G1May 21, 2024
Charcot-Marie-Tooth disease, dominant intermediate A1May 21, 2024
Chilton-Okur-Chung neurodevelopmental syndrome1Dec 12, 2023
Chronic infantile neurological, cutaneous and articular syndrome1May 21, 2024
Ciliary dyskinesia, primary, 49, without situs inversus1May 21, 2024
Clark-Baraitser syndrome1Dec 12, 2023
Classic homocystinuria1May 21, 2024
Cobalamin C disease1May 21, 2024
Colorectal cancer, susceptibility to, 101May 21, 2024
Combined oxidative phosphorylation deficiency 552May 21, 2024
Complex cortical dysplasia with other brain malformations 11May 21, 2024
Complex neurodevelopmental disorder1Dec 12, 2023
Congenital contractures of the limbs and face, hypotonia, and developmental delay1May 21, 2024
Congenital fibrosis of extraocular muscles type 11May 21, 2024
Congenital heart defects and skeletal malformations syndrome1Dec 12, 2023
Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder1Dec 12, 2023
Congenital myopathy1Dec 12, 2023
Congenital stationary night blindness 1A1May 21, 2024
Congenital stationary night blindness 2A1May 21, 2024
Contractures, pterygia, and spondylocarpotarsal fusion syndrome 1A1May 21, 2024
Cowden syndrome 11May 22, 2024
Curry-Jones syndrome3Dec 12, 2023
Cystic fibrosis1May 21, 2024
D-2-hydroxyglutaric aciduria 21May 22, 2024
Deficiency of 2-methylbutyryl-CoA dehydrogenase1May 21, 2024
Deficiency of adenosine deaminase 21Dec 12, 2023
Delpire-McNeill syndrome1Dec 12, 2023
Desmoid disease, hereditary1May 22, 2024
Developmental and epileptic encephalopathy 941Dec 12, 2023
Developmental and epileptic encephalopathy, 131May 21, 2024
Developmental and epileptic encephalopathy, 301Dec 12, 2023
Developmental and epileptic encephalopathy, 411Dec 12, 2023
Developmental and epileptic encephalopathy, 421Dec 12, 2023
Developmental and epileptic encephalopathy, 51May 21, 2024
Developmental and epileptic encephalopathy, 541Dec 12, 2023
Developmental and epileptic encephalopathy, 591Dec 12, 2023
Developmental and epileptic encephalopathy, 691May 21, 2024
Developmental and epileptic encephalopathy, 761Dec 12, 2023
Developmental and epileptic encephalopathy, 812Dec 12, 2023
Developmental delay with or without dysmorphic facies and autism2May 21, 2024
Developmental delay with or without intellectual impairment or behavioral abnormalities1May 21, 2024
Developmental delay with variable intellectual disability and dysmorphic facies1May 21, 2024
Developmental delay, behavioral abnormalities, and neuropsychiatric disorders2May 21, 2024
Developmental delay, impaired speech, and behavioral abnormalities2May 21, 2024
Developmental delay, impaired speech, and behavioral abnormalities, with or without seizures3May 21, 2024
Dias-Logan syndrome1Dec 12, 2023
Diets-Jongmans syndrome1May 21, 2024
Dihydropyrimidine dehydrogenase deficiency1May 21, 2024
Dilated cardiomyopathy 1G9Jul 1, 2024
Donnai-Barrow syndrome1May 21, 2024
Duchenne muscular dystrophy1May 21, 2024
Dyskeratosis congenita, autosomal dominant 31May 21, 2024
Dystonia 28, childhood-onset1Dec 12, 2023
Early-onset myopathy with fatal cardiomyopathy2Dec 12, 2023
Ebstein anomaly1Dec 12, 2023
Ehlers-Danlos syndrome, arthrochalasia type1May 21, 2024
Epidermal nevus3May 22, 2024
Epidermolysis bullosa simplex 5B, with muscular dystrophy1Dec 12, 2023
Epidermolysis bullosa simplex 5C, with pyloric atresia1Dec 12, 2023
Epidermolytic hyperkeratosis 11Dec 12, 2023
Epidermolytic hyperkeratosis 2A, autosomal dominant1May 22, 2024
Epidermolytic nevus3Dec 12, 2023
Epilepsy, familial focal, with variable foci 11May 21, 2024
Episodic ataxia type 23May 21, 2024
Episodic ataxia, type 91Dec 12, 2023
Exostoses, multiple, type 11Dec 12, 2023
FGFR2-related disorder2May 22, 2024
Familial acute necrotizing encephalopathy1Dec 12, 2023
Familial medullary thyroid carcinoma1Dec 12, 2023
Familial partial lipodystrophy, Dunnigan type1May 22, 2024
Familial thoracic aortic aneurysm and aortic dissection1Dec 12, 2023
Feingold syndrome type 11Dec 12, 2023
Focal segmental glomerulosclerosis 81May 22, 2024
Generalized epilepsy with febrile seizures plus, type 21Dec 12, 2023
Glaucoma 3, primary congenital, E1May 22, 2024
Global developmental delay with speech and behavioral abnormalities2Dec 12, 2023
Glomuvenous malformation6May 22, 2024
Growth hormone insensitivity syndrome with immune dysregulation1Dec 12, 2023
Hamartoma of hypothalamus6May 22, 2024
Hemochromatosis type 11Dec 12, 2023
Hemolytic uremic syndrome with DGKE deficiency1Dec 12, 2023
Hemolytic uremic syndrome, atypical, susceptibility to, 12May 22, 2024
Hennekam lymphangiectasia-lymphedema syndrome 12May 22, 2024
Hennekam lymphangiectasia-lymphedema syndrome 216May 22, 2024
Hepatic steatosis1Oct 18, 2024
Hereditary attention deficit-hyperactivity disorder1May 21, 2024
Hereditary breast ovarian cancer syndrome2Dec 12, 2023
Hereditary coproporphyria1Dec 12, 2023
Hereditary factor XI deficiency disease1May 21, 2024
Hereditary hemorrhagic telangiectasia1Dec 12, 2023
Hereditary lymphedema type I4May 22, 2024
Hereditary spastic paraplegia 111May 21, 2024
Hereditary spastic paraplegia 21May 21, 2024
Hogue-Janssens syndrome 11May 21, 2024
Holoprosencephaly 91May 21, 2024
Holt-Oram syndrome1May 21, 2024
Hurler syndrome1May 21, 2024
Hypercholesterolemia, familial, 11May 21, 2024
Hyperinsulinemic hypoglycemia, familial, 11May 22, 2024
Hyperlipoproteinemia, type I1May 21, 2024
Hypertrophic cardiomyopathy 11May 22, 2024
Hypertrophic cardiomyopathy 44May 22, 2024
Hypertrophic cardiomyopathy 95May 22, 2024
Hypotonia, infantile, with psychomotor retardation and characteristic facies 11May 21, 2024
Hypotrichosis-lymphedema-telangiectasia syndrome1May 22, 2024
Hypotrichosis-lymphedema-telangiectasia-renal defect syndrome1May 22, 2024
ITSN1-related neurodevelopmental disorders1Dec 12, 2023
Ichthyosis1Dec 12, 2023
Ichthyosis vulgaris4May 21, 2024
Imerslund-Grasbeck syndrome type 12May 22, 2024
Immunodeficiency 142May 22, 2024
Immunodeficiency 951May 21, 2024
Infantile nephronophthisis1Dec 12, 2023
Inherited neurodegenerative disorder1Dec 12, 2023
Inherited obesity2May 21, 2024
Intellectual developmental disorder 613Dec 12, 2023
Intellectual developmental disorder 622May 21, 2024
Intellectual developmental disorder with dysmorphic facies and ptosis2May 21, 2024
Intellectual developmental disorder with or without epilepsy or cerebellar ataxia1Dec 12, 2023
Intellectual developmental disorder, X-linked 1111May 21, 2024
Intellectual developmental disorder, autosomal dominant 671Dec 12, 2023
Intellectual developmental disorder, autosomal dominant 682May 21, 2024
Intellectual developmental disorder, autosomal recessive 671Dec 12, 2023
Intellectual developmental disorder, autosomal recessive 75, with neuropsychiatric features and variant lissencephaly2May 21, 2024
Intellectual disability, X-linked 12Dec 12, 2023
Intellectual disability, X-linked 961Dec 12, 2023
Intellectual disability, X-linked syndromic, Turner type3May 21, 2024
Intellectual disability, autosomal dominant 131May 21, 2024
Intellectual disability, autosomal dominant 241Dec 12, 2023
Intellectual disability, autosomal dominant 411May 21, 2024
Intellectual disability, autosomal dominant 461Dec 12, 2023
Intellectual disability, autosomal dominant 51Dec 12, 2023
Intellectual disability, autosomal dominant 501May 21, 2024
Intellectual disability, autosomal dominant 521May 21, 2024
Intellectual disability, autosomal dominant 571May 21, 2024
Intellectual disability, autosomal dominant 91Dec 12, 2023
Intellectual disability, autosomal recessive 651May 21, 2024
Intellectual disability-microcephaly-strabismus-behavioral abnormalities syndrome2May 21, 2024
Isolated focal cortical dysplasia type II3May 22, 2024
Juberg-Hayward syndrome1May 21, 2024
KBG syndrome2May 21, 2024
KRIT1-related disorder1Dec 12, 2023
Kabuki syndrome 12May 21, 2024
LIPE-related familial partial lipodystrophy1May 21, 2024
Large congenital melanocytic nevus2May 22, 2024
Leber congenital amaurosis 91May 21, 2024
Lethal congenital contracture syndrome 82May 21, 2024
Leukoencephalopathy-thalamus and brainstem anomalies-high lactate syndrome1Dec 12, 2023
Lewy body dementia1May 21, 2024
Linear nevus sebaceous syndrome1Dec 12, 2023
Loeys-Dietz syndrome 11May 21, 2024
Long QT syndrome1Dec 12, 2023
Long QT syndrome 12Dec 12, 2023
Long QT syndrome 22Dec 12, 2023
Lymphatic malformation 131May 21, 2024
Lymphatic malformation 32Dec 12, 2023
Lymphatic malformation 621May 22, 2024
Lymphatic malformation 75May 22, 2024
Lymphatic malformation 911May 22, 2024
Lymphedema5May 22, 2024
Lymphedema-posterior choanal atresia syndrome8May 22, 2024
Lynch syndrome 12May 21, 2024
Lynch syndrome 42May 21, 2024
Lynch syndrome 52May 21, 2024
Macrocephaly, dysmorphic facies, and psychomotor retardation1May 21, 2024
Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome2May 22, 2024
Macrothrombocytopenia-lymphedema-developmental delay-facial dysmorphism-camptodactyly syndrome1Dec 12, 2023
Maffucci syndrome2May 22, 2024
Mandibular hypoplasia-deafness-progeroid syndrome1May 21, 2024
Mandibulofacial dysostosis-microcephaly syndrome1May 21, 2024
Marshall syndrome1May 21, 2024
Maturity-onset diabetes of the young type 11Dec 12, 2023
Maturity-onset diabetes of the young type 21May 22, 2024
Maturity-onset diabetes of the young type 31May 22, 2024
Maturity-onset diabetes of the young type 81May 22, 2024
McCune-Albright syndrome3May 22, 2024
Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 31May 22, 2024
Metaphyseal chondrodysplasia, Schmid type1Dec 12, 2023
Microcephaly 18, primary, autosomal dominant2May 21, 2024
Microcephaly with or without chorioretinopathy, lymphedema, or intellectual disability1Dec 12, 2023
Mitral valve prolapse, myxomatous 21May 22, 2024
Mucopolysaccharidosis, MPS-III-B1May 21, 2024
Mullegama-Klein-Martinez syndrome1May 21, 2024
Multiple cutaneous and mucosal venous malformations11May 22, 2024
Myofibrillar myopathy 51May 21, 2024
Nephrotic syndrome, type 102May 22, 2024
Nephrotic syndrome, type 131May 22, 2024
Nephrotic syndrome, type 31May 22, 2024
Neurodevelopmental disorder with central hypotonia and dysmorphic facies1May 21, 2024
Neurodevelopmental disorder with dysmorphic facies and thin corpus callosum1Dec 12, 2023
Neurodevelopmental disorder with dysmorphic facies, sleep disturbance, and brain abnormalities2May 21, 2024
Neurodevelopmental disorder with hyperkinetic movements and dyskinesia1May 21, 2024
Neurodevelopmental disorder with hypotonia and variable intellectual and behavioral abnormalities3May 21, 2024
Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures1May 21, 2024
Neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures1May 21, 2024
Neurodevelopmental disorder with hypotonia, seizures, and absent language1Dec 12, 2023
Neurodevelopmental disorder with language delay and variable cognitive abnormalities1May 21, 2024
Neurodevelopmental disorder with microcephaly and dysmorphic facies1May 21, 2024
Neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities1May 21, 2024
Neurodevelopmental disorder with nonspecific brain abnormalities and with or without seizures2May 21, 2024
Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart1Dec 12, 2023
Neurodevelopmental disorder with or without variable brain abnormalities; NEDBA1Dec 12, 2023
Neurodevelopmental disorder with poor language and loss of hand skills1Dec 12, 2023
Neurodevelopmental, jaw, eye, and digital syndrome1Dec 12, 2023
Neurofibromatosis, type 18May 22, 2024
Neuropathy, hereditary motor and sensory, type 6B2Dec 12, 2023
Noonan syndrome2Dec 12, 2023
Noonan syndrome 11Dec 12, 2023
Noonan syndrome 107May 22, 2024
Noonan syndrome 27May 22, 2024
Noonan syndrome 41May 22, 2024
Noonan syndrome 91May 21, 2024
Noonan syndrome-like disorder with loose anagen hair 12May 22, 2024
Nystagmus 1, congenital, X-linked1Dec 12, 2023
O'Donnell-Luria-Rodan syndrome1Dec 12, 2023
Odonto-onycho-dermal dysplasia1May 21, 2024
Ogden syndrome1May 21, 2024
Oto-palato-digital syndrome, type I1May 21, 2024
Oto-palato-digital syndrome, type II1May 21, 2024
Otospondylomegaepiphyseal dysplasia, autosomal recessive1Dec 12, 2023
Overgrowth syndrome4May 22, 2024
Overgrowth syndrome and/or cerebral malformations due to abnormalities in MTOR pathway genes2Dec 12, 2023
PHIP-related behavioral problems-intellectual disability-obesity-dysmorphic features syndrome1May 21, 2024
PIK3CA related overgrowth syndrome27May 22, 2024
PIK3CA-related disorder1Dec 12, 2023
PMM2-congenital disorder of glycosylation1May 22, 2024
PPP1R3F Associated Neurodevelopmental Disorder1May 21, 2024
PTEN hamartoma tumor syndrome2Dec 12, 2023
Pancreatic cancer, susceptibility to, 31May 21, 2024
Parenti-mignot neurodevelopmental syndrome2May 21, 2024
Parkinson disease, late-onset1May 21, 2024
Pelizaeus-Merzbacher disease1May 21, 2024
Periventricular nodular heterotopia 72Dec 12, 2023
Periventricular nodular heterotopia 91Dec 12, 2023
Peroxisome biogenesis disorder 1A (Zellweger)1May 21, 2024
Pfeiffer syndrome2May 22, 2024
Pfeiffer syndrome type 11Dec 12, 2023
Phelan-McDermid syndrome1Dec 12, 2023
Pheochromocytoma1Dec 12, 2023
Pierpont syndrome1May 21, 2024
Pilarowski-Bjornsson syndrome1Dec 12, 2023
Pityriasis rubra pilaris1Dec 12, 2023
Polycystic kidney disease, adult type1May 22, 2024
Polyglandular autoimmune syndrome, type 12May 22, 2024
Pontocerebellar hypoplasia, type 1E2Dec 12, 2023
Postaxial polydactyly-anterior pituitary anomalies-facial dysmorphism syndrome1May 21, 2024
Primary ciliary dyskinesia 32Dec 12, 2023
Primary ciliary dyskinesia 71Dec 12, 2023
Primary dilated cardiomyopathy2Dec 12, 2023
Primrose syndrome1Dec 12, 2023
Progressive myoclonic epilepsy type 71May 21, 2024
Progressive osseous heteroplasia1May 21, 2024
Proteinuria, chronic benign1May 22, 2024
Proteus syndrome1Dec 12, 2023
Pseudohypoparathyroidism type 1B1May 22, 2024
Pseudohypoparathyroidism type I A2May 21, 2024
Pseudopseudohypoparathyroidism4May 22, 2024
Psoriasis 21Dec 12, 2023
Pyogenic granuloma1Dec 12, 2023
Rhabdomyolysis, susceptibility to, 11May 22, 2024
Roberts-SC phocomelia syndrome1May 21, 2024
Rubinstein-Taybi syndrome due to CREBBP mutations1May 21, 2024
SYNGAP1-related developmental and epileptic encephalopathy1Dec 12, 2023
Schaaf-Yang syndrome1Dec 12, 2023
Schuurs-Hoeijmakers syndrome1Dec 12, 2023
Seizures, benign familial infantile, 31Dec 12, 2023
Severe feeding difficulties-failure to thrive-microcephaly due to ASXL3 deficiency syndrome1May 21, 2024
Severe intellectual disability-progressive spastic diplegia syndrome2May 22, 2024
Severe myoclonic epilepsy in infancy1Dec 12, 2023
Short stature with nonspecific skeletal abnormalities1May 21, 2024
Short stature-pituitary and cerebellar defects-small sella turcica syndrome1May 21, 2024
Skeletal overgrowth-craniofacial dysmorphism-hyperelastic skin-white matter lesions syndrome3May 22, 2024
Snijders Blok-Campeau syndrome1Dec 12, 2023
Sotos syndrome1May 21, 2024
Spastic paraplegia, intellectual disability, nystagmus, and obesity1Dec 12, 2023
Spermatogenic failure 461Dec 12, 2023
Spinocerebellar ataxia type 291May 21, 2024
Stickler syndrome type 21May 21, 2024
Stickler syndrome, type 51Dec 12, 2023
Sturge-Weber syndrome3May 22, 2024
Systemic lupus erythematosus1May 21, 2024
Townes-Brocks syndrome 11May 21, 2024
Tuberous sclerosis 16May 22, 2024
Tuberous sclerosis 24May 22, 2024
Tuberous sclerosis syndrome1Dec 12, 2023
Tufted angioma of skin3Dec 12, 2023
Tumor predisposition syndrome 31May 21, 2024
Turnpenny-fry syndrome1Dec 12, 2023
Type 2 diabetes mellitus2May 22, 2024
Tyrosinase-positive oculocutaneous albinism2Dec 12, 2023
Unverricht-Lundborg syndrome1May 21, 2024
Upshaw-Schulman syndrome4May 22, 2024
Van Maldergem syndrome 17May 22, 2024
Van Maldergem syndrome 22May 21, 2024
Vascular malformation17May 22, 2024
Vein of Galen aneurysmal malformation2Dec 12, 2023
Venous malformation1May 22, 2024
Verrucous venous malformation1Dec 12, 2023
Vertebral, cardiac, tracheoesophageal, renal, and limb defects1May 21, 2024
Weill-Marchesani syndrome 12May 21, 2024
Weiss-Kruszka syndrome1Dec 12, 2023
Wiedemann-Steiner syndrome2Dec 12, 2023
Wolfram syndrome 11May 22, 2024
X-linked Alport syndrome1May 22, 2024
X-linked Opitz G/BBB syndrome1May 21, 2024
X-linked intellectual disability1Dec 12, 2023
X-linked intellectual disability, Cantagrel type1May 21, 2024
Xeroderma pigmentosum, group F1May 21, 2024
ZTTK syndrome1May 21, 2024
not provided78May 22, 2024

Testing in GTR

Disease nameNumber of tests
Acrokeratosis verruciformis of Hopf2 tests
Alport syndrome2 tests
Angioosteohypertrophic syndrome2 tests
Arrhythmogenic right ventricular cardiomyopathy3 tests
Atypical hemolytic-uremic syndrome1 test
Autoimmune lymphoproliferative syndrome1 test
Autoimmune lymphoproliferative syndrome, type 1a1 test
Autoinflammation, immune dysregulation, and eosinophilia2 tests
Autosomal dominant Alport syndrome1 test
Autosomal dominant polycystic kidney disease1 test
Autosomal recessive Alport syndrome1 test
Autosomal recessive keratitis-ichthyosis-deafness syndrome1 test
Autosomal recessive polycystic kidney disease1 test
Bannayan-Riley-Ruvalcaba syndrome1 test
Baraitser-Winter syndrome3 tests
Basal cell nevus syndrome 11 test
Basal cell nevus syndrome 21 test
Becker nevus syndrome2 tests
Beckwith-Wiedemann syndrome2 tests
Branchiootorenal Spectrum Disorders1 test
Brugada syndrome3 tests
CLOVES syndrome2 tests
Capillary malformation3 tests
Capillary malformation-arteriovenous malformation 21 test
Cardiac arrhythmia5 tests
Cardioacrofacial dysplasia1 test
Cardioacrofacial dysplasia 11 test
Cardioacrofacial dysplasia 21 test
Cardiofaciocutaneous syndrome 11 test
Cardiomyopathy1 test
Cardiomyopathy, hypertrophic, midventricular, digenic3 tests
Catecholaminergic polymorphic ventricular tachycardia 13 tests
Cerebral arteriovenous malformation1 test
Cerebral cavernous malformation2 tests
Chondrodysplasia punctata2 tests
Coenzyme Q10 deficiency1 test
Coenzyme Q10 deficiency, primary, 31 test
Complex cortical dysplasia with other brain malformations2 tests
Complex cortical dysplasia with other brain malformations 22 tests
Complex cortical dysplasia with other brain malformations 71 test
Complex neurodevelopmental disorder with or without congenital anomalies1 test
Complex vascular malformation with associated anomalies1 test
Congenital disorder of glycosylation1 test
Congenital hemangioma1 test
Congenital ichthyosis of skin1 test
Cowden syndrome1 test
Curry-Jones syndrome3 tests
Darier disease, segmental1 test
Deafness-lymphedema-leukemia syndrome1 test
Developmental and epileptic encephalopathy 1111 test
Developmental and epileptic encephalopathy 6B1 test
Developmental and epileptic encephalopathy, 111 test
Developmental and epileptic encephalopathy, 191 test
Developmental and epileptic encephalopathy, 22 tests
Developmental and epileptic encephalopathy, 272 tests
Developmental and epileptic encephalopathy, 72 tests
Developmental and epileptic encephalopathy, 741 test
Developmental and epileptic encephalopathy, 781 test
Developmental and epileptic encephalopathy, 92 tests
Diabetes mellitus5 tests
Ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomalies1 test
Encephalocraniocutaneous lipomatosis2 tests
Enchondromatosis1 test
Epidermal nevus2 tests
Epidermolytic hyperkeratosis 11 test
Epidermolytic hyperkeratosis 2A, autosomal dominant1 test
Epilepsy1 test
Epilepsy, familial focal, with variable foci 21 test
Epilepsy, familial focal, with variable foci 31 test
Familial aplasia of the vermis1 test
Familial benign pemphigus2 tests
Familial focal epilepsy with variable foci1 test
Familial hyperinsulinism1 test
Familial juvenile hyperuricemic nephropathy type 11 test
Familial steroid-resistant nephrotic syndrome with sensorineural deafness1 test
Focal segmental glomerulosclerosis2 tests
Glomuvenous malformation1 test
Growth hormone insensitivity syndrome with immune dysregulation 2, autosomal dominant1 test
Growth hormone insensitivity with immune dysregulation 1, autosomal recessive1 test
Hemangiomatosis, cutaneous, with associated features1 test
Hemimegalencephaly2 tests
Hennekam lymphangiectasia-lymphedema syndrome 11 test
Hennekam lymphangiectasia-lymphedema syndrome 21 test
Hereditary hemorrhagic telangiectasia1 test
Heterotopia, periventricular, X-linked dominant1 test
Hypereosinophilic syndrome1 test
Hyperinsulinemic hypoglycemia1 test
Hyperkeratotic cutaneous capillary-venous malformations associated with cerebral capillary malformations1 test
Hypertrophic cardiomyopathy1 test
Hypoinsulinemic hypoglycemia and body hemihypertrophy2 tests
Hypotrichosis-lymphedema-telangiectasia syndrome1 test
IMAGe syndrome1 test
Ichthyosis2 tests
Ichthyosis bullosa of Siemens1 test
Immunodeficiency 141 test
Immunodeficiency 362 tests
Immunodeficiency 98 with autoinflammation, X-linked1 test
Infantile myofibromatosis1 test
Isolated focal cortical dysplasia type II2 tests
Keratitis ichthyosis and deafness syndrome1 test
Left ventricular noncompaction2 tests
Linear nevus sebaceous syndrome2 tests
Lissencephaly2 tests
Long QT syndrome3 tests
Lymphangiomyomatosis1 test
Lymphatic malformation1 test
Lymphedema-distichiasis syndrome with renal disease and diabetes mellitus1 test
Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss1 test
Maffucci syndrome2 tests
Marfan syndrome1 test
McCune-Albright syndrome1 test
Megalencephaly-capillary malformation-polymicrogyria syndrome3 tests
Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 13 tests
Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 21 test
Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 32 tests
Melanocytic nevus1 test
Melorheostosis1 test
Microcephaly with or without chorioretinopathy, lymphedema, or intellectual disability1 test
Microcephaly-capillary malformation syndrome1 test
Multiple cutaneous and mucosal venous malformations2 tests
Multisystem disorder1 test
Myofibromatosis1 test
Nephronophthisis1 test
Nephrotic syndrome1 test
Neurocutaneous melanocytosis1 test
Neurodevelopmental disorder1 test
Neurodevelopmental disorder with epilepsy, cataracts, feeding difficulties, and delayed brain myelination2 tests
Neurofibromatosis1 test
Nevus comedonicus syndrome2 tests
Noonan syndrome2 tests
Overgrowth syndrome1 test
PIK3CA related overgrowth syndrome2 tests
PTEN hamartoma tumor syndrome1 test
Parkes Weber syndrome1 test
Periventricular heterotopia with microcephaly, autosomal recessive2 tests
Periventricular nodular heterotopia1 test
Pierson syndrome1 test
Pityriasis rubra pilaris2 tests
Polycystic kidney disease1 test
Porokeratosis2 tests
Porokeratosis 7, multiple types1 test
Primary dilated cardiomyopathy3 tests
Primary lymphedema1 test
Proteus syndrome2 tests
Pyogenic granuloma1 test
RASopathy3 tests
Rare venous malformation1 test
Renal cysts and diabetes syndrome1 test
Renal dysplasia and retinal aplasia1 test
Renal hypoplasia1 test
Renal tubular dysgenesis1 test
Renal-hepatic-pancreatic dysplasia1 test
Segmental overgrowth1 test
Severe neonatal-onset encephalopathy with microcephaly1 test
Short QT syndrome2 tests
Spindle cell hemangioma1 test
Sturge-Weber syndrome1 test
Telangiectasia, hereditary hemorrhagic, type 21 test
Thrombotic microangiopathy1 test
Tuberous sclerosis syndrome2 tests
Tubulointerstitial kidney disease, autosomal dominant, 21 test
Usher syndrome type 2A1 test
VEXAS syndrome2 tests
Van Maldergem syndrome1 test
Vascular anomaly2 tests
Verrucous venous malformation1 test
sporadic cutaneous verruciform xanthoma1 test