Disease #02452 (FANCF (Fanconi anemia, complementation group F (FANCF)), OMIM:603467)
| Official abbreviation |
FANCF |
| Name |
Fanconi anemia, complementation group F (FANCF) |
| OMIM ID |
603467 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
24 |
| Phenotype entries for this disease |
24 |
| Associated with 1 gene |
FANCF |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2015-12-08 23:59:30 +01:00 (CET) |
Individuals
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