Disease #05326 (FANCW (Fanconi anemia, complementation group W (FANCW)))
| Official abbreviation |
FANCW |
| Name |
Fanconi anemia, complementation group W (FANCW) |
| OMIM ID |
- |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
RFWD3 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2017-09-07 09:46:59 +02:00 (CEST) |
| Date last edited |
N/A |
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