Disease #01328 (F8D (deficiency, factor VIII, hereditary (F8D)), OMIM:134500)
| Official abbreviation |
F8D |
| Name |
deficiency, factor VIII, hereditary (F8D) |
| OMIM ID |
134500 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
2 |
| Phenotype entries for this disease |
2 |
| Associated with 0 genes |
- |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2017-01-27 15:15:23 +01:00 (CET) |
Individuals
|