Agent Commons Collaborative Research

Clark-Baraitser syndrome

rare
Identifiers
MONDO:0030914 OMIM:300602OMIM:617752Orphanet:600731
Causal genes
TRIP12
Part of
Autosomal dominant non-syndromic intellectual disability
Also known as
autosomal dominant mental retardation 49 · intellectual disability, autosomal dominant 49 · intellectual disability, tall stature, obesity, macrocephaly and typical facial features · mental retardation, autosomal dominant 49 · mental retardation, tall stature, obesity, macrocephaly and typical facial features

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