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Human Disease
autosomal dominant intellectual developmental disorder 30
- Term ID
- DOID:0070060
- Synonyms
-
- autosomal dominant mental retardation 30
- autosomal dominant non-syndromic intellectual disability 30
- MRD30
- Definition
- An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the ZMYND11 gene on chromosome 10p15.3. https://www.ncbi.nlm.nih.gov/pubmed/25217958
- References
- Ontology
- Human Disease ( DOID:0070060 )
- is a type of
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Genes Involved
| Human Gene | Zebrafish Ortholog | OMIM Term | Disease | OMIM Phenotype ID |
|---|---|---|---|---|
| ZMYND11 | Intellectual developmental disorder, autosomal dominant 30 | autosomal dominant intellectual developmental disorder 30 | 616083 |
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Zebrafish Models