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

intellectual disability, autosomal recessive 34

Disease Summary
Associated Targets (1)
Tbio

1


Explore Associated Targets
Mondo Description Any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the CRADD gene.
Uniprot Description A disorder characterized by significantly below average general intellectual functioning associated with impairments in adaptive behavior and manifested during the developmental period. MRT34 is a non-syndromic form. Affected individuals have mildly delayed development and significantly impaired cognitive function, precluding independent living and self-care. Speech is rudimentary, but articulate; autism is not present.
Mondo Term and Equivalent IDs
MONDO:0013785:  intellectual disability, autosomal recessive 34
NCIT:C153179: 
UMLS:C3281044: 
GWAS Targets (0)
No GWAS traits found
Target Novelty (Tin-x)
No novelty measurements found