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Williams syndrome

Disease Summary
Associated Targets (28)
Tbio

21

Tdark

4

Tchem

3


Explore Associated Targets
Mondo Description Williams syndrome is a rare genetic multisystemic neurodevelopmental disorder characterized by a distinct facial appearance, cardiac anomalies (most frequently supravalvular aortic stenosis), cognitive and developmental abnormalities, and connective tissue abnormalities (such as joint laxity)
Mondo Term and Equivalent IDs
MONDO:0008678:  Williams syndrome
GARD:0007891: 
MESH:D018980: 
NCIT:C85232: 
Orphanet:904: 
SCTID:63247009: 
UMLS:C0175702: 
GWAS Targets (0)
No GWAS traits found
Disease Hierarchy
Parents
Tbio

4331

Tchem

803

Tdark

604

Tclin

358

Tbio

2250

Tchem

535

Tdark

340

Tclin

240

Tbio

1763

Tchem

284

Tdark

193

Tclin

124

Tbio

558

Tchem

165

Tclin

114

Tdark

63

Tbio

640

Tchem

110

Tclin

48

Tdark

39

Tbio

109

Tchem

34

Tclin

33

Tdark

5

Tbio

78

Tclin

20

Tchem

19

Tdark

5

Tbio

31

Tchem

8

Tdark

4

Tclin

1

Children
Target Novelty (Tin-x)