von Willebrand's disease 1
von Willebrand's disease characterized by quantitative partial deficiency of circulating VWF that has material basis in heterozygous mutation in the VWF gene on chromosome 12p13
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von Willebrand's disease 1
Summary
von Willebrand's disease 1 is a rare disease[1].
Key Facts
- von Willebrand's disease 1's instance of is recorded as rare disease[2].
- von Willebrand's disease 1's instance of is recorded as class of disease[3].
- von Willebrand's disease 1's subclass of is recorded as von Willebrand's disease[4].
- von Willebrand's disease 1's MeSH descriptor ID is recorded as D056725[5].
- von Willebrand's disease 1's OMIM ID is recorded as 193400[6].
- von Willebrand's disease 1's MeSH tree code is recorded as C15.378.100.100.900.100[7].
- von Willebrand's disease 1's MeSH tree code is recorded as C15.378.100.141.900.100[8].
- von Willebrand's disease 1's MeSH tree code is recorded as C15.378.463.920.100[9].
- von Willebrand's disease 1's MeSH tree code is recorded as C16.320.099.920.100[10].
- von Willebrand's disease 1's Disease Ontology ID is recorded as DOID:0060573[11].
- von Willebrand's disease 1's Orphanet ID is recorded as 166078[12].
- von Willebrand's disease 1's NCI Thesaurus ID is recorded as C131685[13].
- von Willebrand's disease 1's health specialty is recorded as hematology[14].
- von Willebrand's disease 1's health specialty is recorded as medical genetics[15].
- von Willebrand's disease 1's genetic association is recorded as VWF[16].
- von Willebrand's disease 1's exact match is recorded as http://identifiers.org/doid/DOID:0060573[17].
- von Willebrand's disease 1's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060573[18].
- von Willebrand's disease 1's UMLS CUI is recorded as C1264039[19].
- von Willebrand's disease 1's on focus list of Wikimedia project is recorded as WikiProject Medicine[20].
- von Willebrand's disease 1's Mondo ID is recorded as MONDO_0008668[21].
- von Willebrand's disease 1's UniProt disease ID is recorded as DI-02903[22].