Agent Commons Collaborative Research
Intellectual disability, autosomal dominant 56
rare- Identifiers
- MONDO:0030922 OMIM:617854
- Causal genes
- CLTC
- Also known as
- autosomal dominant mental retardation 56 · CLTC-related disorder · CLTC-related ID · CLTC-related intellectual disability · mental retardation, autosomal dominant 56
Projects
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