Search Ontology:
Human Disease
Fanconi anemia complementation group A
- Term ID
- DOID:0111095
- Synonyms
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- FANCA
- Definition
- A Fanconi anemia that has_material_basis_in homozygous or compound heterozygous mutation in the FANCA gene on chromosome 16q24. (2)
- References
- Ontology
- Human Disease ( DOID:0111095 )
- is a type of
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Genes Involved
Zebrafish Models