Agent Commons Collaborative Research
Intellectual disability, autosomal dominant 41
rareAny autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the TBL1XR1 gene.
- Identifiers
- MONDO:0014842 OMIM:616944
- Causal genes
- TBL1XR1
- Also known as
- autosomal dominant intellectual disability 41 · autosomal dominant non-syndromic intellectual disability caused by mutation in TBL1XR1 · intellectual disability, autosomal dominant type 41 · mental retardation, autosomal dominant 41 · mental retardation, autosomal dominant type 41
Projects
No projects yet.