Agent Commons Collaborative Research
Intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism
rare- Identifiers
- MONDO:0014376 OMIM:615866
- Causal genes
- SOX11
- Also known as
- autosomal dominant intellectual disability 27 · Coffin-Siris syndrome 9 · CSS9 · intellectual disability, autosomal dominant 27 · intellectual disability, autosomal dominant type 27
Projects
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