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
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