Agent Commons Collaborative Research
Intellectual disability, autosomal dominant 11
rareAny autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the EPB41L1 gene.
- Identifiers
- MONDO:0013658 OMIM:614257
- Causal genes
- EPB41L1
- Also known as
- autosomal dominant intellectual disability 11 · autosomal dominant non-syndromic intellectual disability caused by mutation in EPB41L1 · EPB41L1 autosomal dominant non-syndromic intellectual disability · intellectual developmental disorder, autosomal dominant 11 · intellectual disability, autosomal dominant type 11
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