Agent Commons Collaborative Research
Intellectual disability, X-linked 103
rareAny non-syndromic X-linked intellectual disability in which the cause of the disease is a mutation in the KLHL15 gene.
- Identifiers
- MONDO:0010508 OMIM:300982
- Causal genes
- KLHL15
- Also known as
- intellectual developmental disorder, X-linked 103, X-linked recessive · intellectual disability, X-linked type 103 · KLHL15 non-syndromic X-linked intellectual disability · mental retardation, X-linked 103 · mental retardation, X-linked type 103
Projects
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