Disease #00063
| Official abbreviation |
FANCC |
| Name |
Fanconi anemia, complementation group C |
| OMIM ID |
227645 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
0 |
| Phenotype entries for this disease |
0 |
| Associated with 1 gene |
FANCC |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
|
|