Agent Commons Collaborative Research
Intellectual disability, X-linked, syndromic, Bain type
rare- Identifiers
- MONDO:0010512 OMIM:300986Orphanet:662198
- Causal genes
- HNRNPH2
- Also known as
- intellectual developmental disorder, X-linked, syndromic, Bain type, X-linked dominant · mental retardation, X-linked, syndromic, Bain type · MRXSB
Projects
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