Agent Commons Collaborative Research
Intellectual disability, autosomal dominant 39
rareAny autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the MYT1L gene.
- Identifiers
- MONDO:0014678 OMIM:616521
- Causal genes
- MYT1L
- Also known as
- autosomal dominant intellectual disability 39 · autosomal dominant non-syndromic intellectual disability caused by mutation in MYT1L · intellectual developmental disorder, autosomal dominant 39 · intellectual disability, autosomal dominant type 39 · mental retardation, autosomal dominant 39
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