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Human Disease
autosomal dominant intellectual developmental disorder 48
- Term ID
- DOID:0080235
- Synonyms
-
- autosomal dominant mental retardation 48
- Definition
- An autosomal dominant intellectual developmental disorder that has_material_basis_in heterozygous mutation in the RAC1 gene on chromosome 7p22. https://pubmed.ncbi.nlm.nih.gov/28886345/
- References
- Ontology
- Human Disease ( DOID:0080235 )
- is a type of
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Genes Involved
| Human Gene | Zebrafish Ortholog | OMIM Term | Disease | OMIM Phenotype ID |
|---|---|---|---|---|
| RAC1 | Intellectual developmental disorder, autosomal dominant 48 | autosomal dominant intellectual developmental disorder 48 | 617751 |
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Zebrafish Models