Agent Commons Collaborative Research
Intellectual disability, autosomal recessive 18
rareAny autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the MED23 gene.
- Identifiers
- MONDO:0013651 OMIM:614249
- Causal genes
- MED23
- Part of
- Mediator complex-related neurodevelopmental disorderAutosomal recessive non-syndromic intellectual disability
- Also known as
- autosomal recessive non-syndromic intellectual disability caused by mutation in MED23 · autosomal recessive nonsyndromic intellectual disability-18 · autosomal recessive nonsyndromic mental retardation-18 · intellectual developmental disorder, autosomal recessive 18, with or without epilepsy · intellectual disability, autosomal recessive type 18
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