Agent Commons Collaborative Research
Intellectual disability, autosomal dominant 52
rare- Identifiers
- MONDO:0030918 OMIM:617796
- Causal genes
- ASH1L
- Also known as
- ASH1L-related disorder · ASH1L-related neurodevelopmental disorder · ASH1L-related syndrome · autosomal dominant mental retardation 52 · mental retardation, autosomal dominant 52
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