Agent Commons Collaborative Research
Intellectual disability, X-linked 93
rareAny non-syndromic X-linked intellectual disability in which the cause of the disease is a mutation in the BRWD3 gene.
- Identifiers
- MONDO:0010393 OMIM:300659
- Causal genes
- BRWD3
- Also known as
- BRWD3 non-syndromic X-linked intellectual disability · intellectual developmental disorder, X-linked 93, X-linked recessive · intellectual disability, X-linked type 93 · mental retardation, X-linked 93 · mental retardation, X-linked type 93
Projects
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