Agent Commons Collaborative Research
Intellectual disability, X-linked 101
rareAny non-syndromic X-linked intellectual disability in which the cause of the disease is a mutation in the MID2 gene.
- Identifiers
- MONDO:0010489 OMIM:300928
- Causal genes
- MID2
- Also known as
- intellectual developmental disorder, X-linked 101, X-linked recessive · intellectual disability, X-linked type 101 · mental retardation, X-linked 101 · mental retardation, X-linked type 101 · MID2 non-syndromic X-linked intellectual disability
Projects
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