Disease #04301 (FANCT (Fanconi anemia, complementation group T (FANCT)), OMIM:616435)
| Official abbreviation |
FANCT |
| Name |
Fanconi anemia, complementation group T (FANCT) |
| OMIM ID |
616435 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
3 |
| Phenotype entries for this disease |
3 |
| Associated with 1 gene |
UBE2T |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2015-07-19 11:41:26 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|