Intellectual disability, autosomal dominant 33

rare

Any autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the DPP6 gene.

Identifiers: MONDO:0014580 OMIM:616311
Causal genes: DPP6
Part of: Autosomal dominant non-syndromic intellectual disability
Also known as: autosomal dominant intellectual disability 33 · autosomal dominant non-syndromic intellectual disability caused by mutation in DPP6 · DPP6 autosomal dominant non-syndromic intellectual disability · intellectual disability, autosomal dominant type 33 · mental retardation, autosomal dominant 33

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