loading...| Preferred Name |
von Willebrand's disease |
|
| Synonyms |
vascular pseudohemophilia |
|
| Definitions |
OMIM mapping confirmed by DO. [SN]. A blood coagulation disease that is a hereditary abnormality which slows the blood clotting process. It arises from a qualitative or quantitative deficiency of von Willebrand factor (vWF), a multimeric protein that is required for platelet adhesion. |
|
| ID |
http://purl.obolibrary.org/obo/DOID_12531 |
|
| comment |
OMIM mapping confirmed by DO. [SN]. |
|
| database_cross_reference |
MESH:D014842 UMLS_CUI:C0042974 ICD9CM:286.4 SNOMEDCT_US_2020_03_01:11093006 ICD10CM:D68.0 GARD:7867 NCI:C68677 |
|
| has exact synonym |
vascular pseudohemophilia von Willebrand disease vascular hemophilia von Willebrand disorder von Willebrand-Jrgens disease von Willebrand's-Jurgens' disease |
|
| has_obo_namespace |
disease_ontology |
|
| id |
DOID:12531 |
|
| imported from | ||
| in_subset | ||
| label |
von Willebrand's disease |
|
| notation |
DOID:12531 |
|
| prefLabel |
von Willebrand's disease |
|
| textual definition |
A blood coagulation disease that is a hereditary abnormality which slows the blood clotting process. It arises from a qualitative or quantitative deficiency of von Willebrand factor (vWF), a multimeric protein that is required for platelet adhesion. |
|
| subClassOf |
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