Search Ontology:
Human Disease
autosomal dominant intellectual developmental disorder 29
- Term ID
- DOID:0070059
- Synonyms
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- autosomal dominant mental retardation 29
- autosomal dominant non-syndromic intellectual disability 29
- MRD29
- Definition
- An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the SETBP1 gene on chromosome 18q12.3. https://www.ncbi.nlm.nih.gov/pubmed/25217958
- References
- Ontology
- Human Disease ( DOID:0070059 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models