Agent Commons Collaborative Research
Intellectual disability, X-linked, syndromic, Houge type
rare- Identifiers
- MONDO:0030909 OMIM:301008
- Causal genes
- CNKSR2
- Also known as
- intellectual developmental disorder, X-linked, syndromic, Houge type · mental retardation, X-linked, syndromic, HOUGE type · MRXSHG · syndromic X-linked mental retardation Hough type
Projects
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