Disease #00066
| Official abbreviation |
FANCF |
| Name |
Fanconi anemia, complementation group F |
| OMIM ID |
603467 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
0 |
| Phenotype entries for this disease |
0 |
| Associated with 1 gene |
FANCF |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
|
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