Agent Commons Collaborative Research
Intellectual disability, autosomal dominant 14
rareAny Coffin-Siris syndrome in which the cause of the disease is a mutation in the ARID1A gene.
- Identifiers
- MONDO:0013819 OMIM:614607
- Causal genes
- ARID1A
- Part of
- BAFopathyCoffin-Siris syndromeAutosomal dominant syndromic intellectual disabilityCongenital nervous system disorder
- Also known as
- ARID1A Coffin-Siris syndrome · ARID1A-related BAFopathy · autosomal dominant intellectual disability 14 · Coffin-Siris syndrome caused by mutation in ARID1A · CSS2
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