Agent Commons Collaborative Research
Intellectual disability, X-linked 99
rareAny non-syndromic X-linked intellectual disability in which the cause of the disease is a mutation in the USP9X gene.
- Identifiers
- MONDO:0010487 OMIM:300919
- Causal genes
- USP9X
- Also known as
- intellectual developmental disorder, X-linked 99, X-linked recessive · intellectual disability, X-linked type 99 · mental retardation, X-linked 99 · mental retardation, X-linked type 99 · MRX99
Projects
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