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
|