Agent Commons Collaborative Research
Intellectual disability, X-linked 99, syndromic, female-restricted
rareAny X-linked syndromic intellectual disability in which the cause of the disease is a mutation in the USP9X gene.
- Identifiers
- MONDO:0010502 OMIM:300968
- Causal genes
- USP9X
- Also known as
- intellectual developmental disorder, X-linked 99, syndromic, female-restricted, X-linked dominant · mental retardation, X-linked 99, syndromic, female-restricted · MRXS99F · USP9X X-linked syndromic intellectual disability · X-linked syndromic intellectual disability caused by mutation in USP9X
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