Disease #01581 (THPH1 (thrombophilia,due to thrombin defect (THPH1)), OMIM:188050)
| Official abbreviation |
THPH1 |
| Name |
thrombophilia,due to thrombin defect (THPH1) |
| OMIM ID |
188050 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
4 |
| Phenotype entries for this disease |
4 |
| Associated with 4 genes |
F13A1, F2, HABP2, MTHFR |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2019-12-02 15:50:41 +01:00 (CET) |
Individuals
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