Search Ontology:
Human Disease
Fanconi anemia complementation group R
- Term ID
- DOID:0111090
- Synonyms
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- FANCR
- Definition
- A Fanconi anemia that has_material_basis_in heterozygous mutation in the RAD51 gene on chromosome 15q15. https://www.ncbi.nlm.nih.gov/pubmed/26681308
- References
- Ontology
- Human Disease ( DOID:0111090 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models