| Term Name: | Fanconi anemia complementation group A |
|---|---|
| Synonyms: | FANCA |
| Definition: | A Fanconi anemia that has_material_basis_in homozygous or compound heterozygous mutation in the FANCA gene on chromosome 16q24. |
| Ontology: | Human Disease [DOID:0111095] ( DOID:0111095 ) |