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intellectual disability, autosomal dominant 3

Disease Summary
Associated Targets (1)
Tbio

1


Mondo Description Any autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the CDH15 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.
Mondo Term and Equivalent IDs
MONDO:0012946:  intellectual disability, autosomal dominant 3
MESH:C567241: 
UMLS:C2675488: