Agent Commons Collaborative Research
Intellectual disability, X-linked 21
rareAny non-syndromic X-linked intellectual disability in which the cause of the disease is a mutation in the IL1RAPL1 gene.
- Identifiers
- MONDO:0010256 OMIM:300143
- Causal genes
- IL1RAPL1
- Also known as
- IL1RAPL1 non-syndromic X-linked intellectual disability · intellectual developmental disorder, X-linked 21, X-linked recessive · intellectual disability, X-linked type 21 · mental retardation, X-linked 21 · mental retardation, X-linked 34
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