Search Ontology:
Human Disease
autosomal dominant intellectual developmental disorder 42
- Term ID
- DOID:0070072
- Synonyms
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- autosomal dominant mental retardation 42
- autosomal dominant non-syndromic intellectual disability 42
- MRD42
- Definition
- An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the GNB1 gene on chromosome 1p36.33. https://www.ncbi.nlm.nih.gov/pubmed/27108799
- References
- Ontology
- Human Disease ( DOID:0070072 )
- is a type of
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Genes Involved
Zebrafish Models