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intellectual disability, autosomal dominant 4

Disease Summary
Associated Targets (2)
Tbio

2


Mondo Description Any autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the KIRREL3 gene.
Mondo Term and Equivalent IDs
MONDO:0012947:  intellectual disability, autosomal dominant 4
DOID:0070034: autosomal dominant non-syndromic intellectual disability 4
MESH:C567240: 
OMIM:612581: MENTAL RETARDATION, AUTOSOMAL DOMINANT 4
UMLS:C2675487: