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