Disease #04471 (Dysfibrinogenemia, congenital, OMIM:616004)
| Official abbreviation |
- |
| Name |
Dysfibrinogenemia, congenital |
| OMIM ID |
616004 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 3 genes |
FGA, FGB, FGG |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2015-09-23 10:25:22 +02:00 (CEST) |
| Date last edited |
N/A |
Individuals
|