Disease #04305 (FANCR (Fanconi anemia, complementation group R (FANCR)), OMIM:617244)
| Official abbreviation |
FANCR |
| Name |
Fanconi anemia, complementation group R (FANCR) |
| OMIM ID |
617244 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
RAD51 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2015-07-19 11:50:53 +02:00 (CEST) |
| Date last edited |
2021-12-30 17:20:17 +01:00 (CET) |
Individuals
|