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Human Disease
autosomal dominant intellectual developmental disorder 41
- Term ID
- DOID:0070071
- Synonyms
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- autosomal dominant mental retardation 41
- autosomal dominant non-syndromic intellectual disability 41
- MRD41
- Definition
- An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the TBL1XR1 gene on chromosome 3q26.32. https://www.ncbi.nlm.nih.gov/pubmed/25102098
- References
- Ontology
- Human Disease ( DOID:0070071 )
- is a type of
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Genes Involved
Zebrafish Models