Disease #01582 (THPH2 (thrombophilia, due to activated protein C resistance (THPH2)), OMIM:188055)
Official abbreviation |
THPH2 |
Name |
thrombophilia, due to activated protein C resistance (THPH2) |
OMIM ID |
188055 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
7 |
Phenotype entries for this disease |
7 |
Associated with 1 gene |
F5 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
Date last edited |
2019-12-02 15:51:36 +01:00 (CET) |
Individuals
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