Search Ontology:
Human Disease
Fanconi anemia complementation group U
- Term ID
- DOID:0111085
- Synonyms
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- FANCU
- Definition
- A Fanconi anemia that has_material_basis_in homozygous mutation in the XRCC2 gene on chromosome 7q36. https://www.ncbi.nlm.nih.gov/pubmed/22232082
- References
- Ontology
- Human Disease ( DOID:0111085 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models