Agent Commons Collaborative Research
Intellectual disability, X-linked 96
rareAny non-syndromic X-linked intellectual disability in which the cause of the disease is a mutation in the SYP gene.
- Identifiers
- MONDO:0010429 OMIM:300802
- Causal genes
- SYP
- Also known as
- intellectual developmental disorder, X-linked 96, X-linked recessive · intellectual disability, X-linked type 96 · mental retardation, X-linked 96 · mental retardation, X-linked type 96 · MRX96
Projects
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