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Biological and Environmental Research Ontology
Last uploaded:
December 23, 2022
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| Preferred Name | von Willebrand Disease, Type 1 | |
| Synonyms |
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| Definitions |
An autosomally inherited (generally dominant) coagulation disorder characterized by quantitative partial deficiency of circulating von Willebrand factor (VWF) which account for 60 to 80% of cases of von Willebrand disease. It is characterized by mild to moderate quantitative deficiencies of VWF and factor VIII, which are coordinately reduced from normal plasma levels. |
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| ID |
http://purl.obolibrary.org/obo/NCIT_C131685 |
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| ALT_DEFINITION |
An autosomally inherited (generally dominant) coagulation disorder characterized by quantitative partial deficiency of circulating von Willebrand factor (VWF) which account for 60 to 80% of cases of von Willebrand disease. It is characterized by mild to moderate quantitative deficiencies of VWF and factor VIII, which are coordinately reduced from normal plasma levels.
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| code |
C131685
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| Contributing_Source |
NICHD
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| definition |
An autosomally inherited (generally dominant) coagulation disorder characterized by quantitative partial deficiency of circulating von Willebrand factor (VWF) which account for 60 to 80% of cases of von Willebrand disease. It is characterized by mild to moderate quantitative deficiencies of VWF and factor VIII, which are coordinately reduced from normal plasma levels.
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| in_subset | ||
| label |
von Willebrand Disease, Type 1
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| Preferred_Name |
von Willebrand Disease, Type 1
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| prefixIRI |
NCIT:C131685
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| prefLabel |
von Willebrand Disease, Type 1
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| Semantic_Type |
Disease or Syndrome
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| UMLS_CUI |
C1264039
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| subClassOf |
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