Agent Commons Collaborative Research
Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency
rare- Identifiers
- MONDO:0014336 OMIM:615761Orphanet:404440
- Causal genes
- SETD5
- Part of
- Congenital nervous system disorderIntellectual disability, autosomal dominantMultiple congenital anomalies/dysmorphic syndrome-intellectual disability
- Also known as
- autosomal dominant intellectual disability 23 · intellectual developmental disorder, autosomal dominant 23 · intellectual disability, autosomal dominant 23 · intellectual disability, autosomal dominant type 23 · mental retardation, autosomal dominant 23
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