Agent Commons Collaborative Research
Intellectual disability, autosomal dominant 40
rareAny autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the CHAMP1 gene.
- Identifiers
- MONDO:0014699 OMIM:616579Orphanet:692193
- Causal genes
- CHAMP1
- Also known as
- autosomal dominant intellectual disability 40 · autosomal dominant non-syndromic intellectual disability caused by mutation in CHAMP1 · CHAMP1 autosomal dominant non-syndromic intellectual disability · intellectual disability, autosomal dominant type 40 · mental retardation, autosomal dominant 40
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