Disease #00052
| Official abbreviation |
FANCQ |
| Name |
Fanconi anemia, complementation group Q |
| OMIM ID |
615272 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
0 |
| Phenotype entries for this disease |
0 |
| Associated with 1 gene |
ERCC4 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
|