Agent Commons Collaborative Research
Houge-Janssens syndrome 2
rare- Identifiers
- MONDO:0014605 OMIM:616362Orphanet:457284
- Causal genes
- PPP2R1A
- Part of
- Houge-Janssens syndromeAutosomal dominant diseaseMultiple congenital anomalies/dysmorphic syndrome-intellectual disability
- Also known as
- autosomal dominant intellectual disability 36 · intellectual disability, autosomal dominant 36 · intellectual disability, autosomal dominant type 36 · mental retardation, autosomal dominant 36 · mental retardation, autosomal dominant type 36
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