Search Ontology:
Human Disease
autosomal dominant intellectual developmental disorder 13
- Term ID
- DOID:0070043
- Synonyms
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- autosomal dominant mental retardation 13
- autosomal dominant non-syndromic intellectual disability 13
- mental retardation, autosomal dominant 13, with neuronal migration defects
- MRD13
- Definition
- An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the DYNC1H1 gene on chromosome 14q32.31. https://www.ncbi.nlm.nih.gov/pubmed/21076407
- References
- Ontology
- Human Disease ( DOID:0070043 )
- is a type of
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Genes Involved
Zebrafish Models