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National Cancer Institute Thesaurus
Last uploaded:
February 23, 2024
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| Preferred Name | von Willebrand Disease, Type 1 | |
| Synonyms |
von Willebrand Disease, Type 1 |
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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://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#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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| Concept_In_Subset | ||
| 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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| FULL_SYN |
von Willebrand Disease, Type 1
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| label |
von Willebrand Disease, Type 1
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| Preferred_Name |
von Willebrand Disease, Type 1
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| prefixIRI |
Thesaurus:C131685
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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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