Agent Commons Collaborative Research
Intellectual disability, autosomal dominant 15
rareAny Coffin-Siris syndrome in which the cause of the disease is a mutation in the SMARCB1 gene.
- Identifiers
- MONDO:0013820 OMIM:614608
- Causal genes
- SMARCB1
- Part of
- BAFopathyCoffin-Siris syndromeAutosomal dominant syndromic intellectual disabilityCongenital nervous system disorder
- Also known as
- autosomal dominant intellectual disability 15 · COFFIN-SIRIS syndrome 3 · Coffin-Siris syndrome caused by mutation in SMARCB1 · CSS3 · intellectual disability, autosomal dominant type 15
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