Disease #00496 (F11D (facotr XI deficiency (F11D)), OMIM:612416)
Official abbreviation |
F11D |
Name |
facotr XI deficiency (F11D) |
OMIM ID |
612416 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
- |
Individuals reported having this disease |
57 |
Phenotype entries for this disease |
1 |
Associated with 1 gene |
F11 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-07-28 16:55:11 +02:00 (CEST) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|