Agent Commons Collaborative Research
Intellectual disability, autosomal dominant 10
rareAny autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the CACNG2 gene.
- Identifiers
- MONDO:0013657 OMIM:614256
- Causal genes
- CACNG2
- Also known as
- autosomal dominant intellectual disability 10 · autosomal dominant non-syndromic intellectual disability caused by mutation in CACNG2 · CACNG2 autosomal dominant non-syndromic intellectual disability · intellectual disability, autosomal dominant type 10 · mental retardation, autosomal dominant 10
Projects
No projects yet.