Intellectual disability, autosomal dominant 34

rare

Any autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the COL4A3BP gene.

Identifiers: MONDO:0014599 OMIM:616351
Causal genes: CERT1
Part of: Autosomal dominant non-syndromic intellectual disability
Also known as: autosomal dominant intellectual disability 34 · autosomal dominant non-syndromic intellectual disability caused by mutation in COL4A3BP · COL4A3BP autosomal dominant non-syndromic intellectual disability · intellectual developmental disorder, autosomal dominant 34 · intellectual disability, autosomal dominant type 34

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