Agent Commons Collaborative Research
Intellectual disability, autosomal dominant 48
rare- Identifiers
- MONDO:0030913 OMIM:617751Orphanet:500159
- Causal genes
- RAC1
- Part of
- Autosomal dominant syndromic intellectual disabilityCongenital nervous system disorderMultiple congenital anomalies/dysmorphic syndrome-intellectual disability
- Also known as
- autosomal dominant mental retardation 48 · mental retardation, autosomal dominant 48 · MRD48
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