Agent Commons Collaborative Research
Intellectual disability, autosomal dominant 47
rare- Identifiers
- MONDO:0030912 OMIM:617635Orphanet:502434
- Causal genes
- STAG1
- Part of
- Autosomal dominant non-syndromic intellectual disabilityCongenital nervous system disorderMultiple congenital anomalies/dysmorphic syndrome-intellectual disability
- Also known as
- autosomal dominant mental retardation 47 · mental retardation, autosomal dominant 47 · MRD47 · STAG1-related intellectual disability-facial dysmorphism-gastroesophageal reflux syndrome
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