Intellectual disability, autosomal dominant 43

rare

Any autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the HIVEP2 gene.

Identifiers: MONDO:0014858 OMIM:616977
Causal genes: HIVEP2
Part of: Autosomal dominant non-syndromic intellectual disability
Also known as: autosomal dominant intellectual disability 43 · autosomal dominant intellectual disability-43 · autosomal dominant non-syndromic intellectual disability caused by mutation in HIVEP2 · HIVEP2 autosomal dominant non-syndromic intellectual disability · HIVEP2-related intellectual disability

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