You are using an outdated browser. Please upgrade your browser to improve your experience.

autosomal recessive non-syndromic intellectual disability

Disease Summary
Associated Targets (42)
Tbio

30

Tchem

6

Tclin

3

Tdark

3


Explore Associated Targets
Mondo Description Autosomal recessive form of non-syndromic intellectual disability.
Disease Ontology Description A non-syndromic intellectual disability characterized by an autosomal recessive inheritance pattern.
Mondo Term and Equivalent IDs
MONDO:0019502:  autosomal recessive non-syndromic intellectual disability
OMIMPS:249500: 
Orphanet:88616: 
UMLS:CN206293: 
GWAS Targets (0)
No GWAS traits found
Disease Hierarchy
Parents
Tbio

4331

Tchem

803

Tdark

604

Tclin

358

Tbio

1892

Tchem

356

Tdark

238

Tclin

136

Children
Target Novelty (Tin-x)