Disease #03542 (FANCG (Fanconi anemia, complementation group G (FANCG)), OMIM:614082)
| Official abbreviation |
FANCG |
| Name |
Fanconi anemia, complementation group G (FANCG) |
| OMIM ID |
614082 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
154 |
| Phenotype entries for this disease |
132 |
| Associated with 1 gene |
FANCG |
| 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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