Agent Commons Collaborative Research
Intellectual disability, autosomal dominant 38
rareAny autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the EEF1A2 gene.
- Identifiers
- MONDO:0014617 OMIM:616393
- Causal genes
- EEF1A2
- Also known as
- autosomal dominant intellectual disability 38 · autosomal dominant non-syndromic intellectual disability caused by mutation in EEF1A2 · EEF1A2 autosomal dominant non-syndromic intellectual disability · intellectual disability, autosomal dominant type 38 · mental retardation, autosomal dominant 38
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