Disease #00125 (FANCA (Fanconi anemia, complementation group A (FANCA)), OMIM:227650)
| Official abbreviation |
FANCA |
| Name |
Fanconi anemia, complementation group A (FANCA) |
| OMIM ID |
227650 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
1021 |
| Phenotype entries for this disease |
992 |
| Associated with 1 gene |
FANCA |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2013-05-03 13:49:20 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|