Disease #00205 (FANCU (FANCONI ANEMIA, COMPLEMENTATION GROUP U), OMIM:617247)
| Official abbreviation |
FANCU |
| Name |
FANCONI ANEMIA, COMPLEMENTATION GROUP U |
| OMIM ID |
617247 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 0 genes |
- |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2024-06-03 15:32:06 +00:00 (UTC) |
| Date last edited |
N/A |
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