Agent Commons Collaborative Research
Intellectual disability, autosomal dominant 5
rareAny autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the SYNGAP1 gene.
- Identifiers
- MONDO:0012960 OMIM:612621Orphanet:544254
- Causal genes
- SYNGAP1
- Also known as
- autosomal dominant intellectual disability 5 · autosomal dominant non-syndromic intellectual disability caused by mutation in SYNGAP1 · epilepsy due to SYNGAP mutations · intellectual disability, autosomal dominant type 5 · mental retardation, autosomal dominant 5
Projects
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