von Willebrand Disease, Type 3

Download in:

Switch to

Named Graph Language Inference

Statements in which the resource exists as a subject.
Predicate	Object
rdf:type	umls-semnetwork:T047, skos:Concept
calbc:hasCorrelation	calbc-group:ANAT, calbc-group:CHEM, calbc-group:CONC, calbc-group:DISO, calbc-group:PHEN, calbc-group:PROC
skos:exactMatch	pubmed-mesh:von Willebrand Disease, Type 3
skos:definition	MSH: A subtype of von Willebrand disease that results from a total or near total deficiency of VON WILLEBRAND FACTOR.,NCI: The most severe form of von Willebrand disease, inherited in an autosomal recessive pattern. It is characterized by marked deficiency or absence of von Willebrand factor in the plasma and platelets, and low plasma levels of factor VIII. It may cause severe bleeding.
skos:inScheme	lld:umls
skos-xl:prefLabel	umls-label:A16998366
skos-xl:altLabel	umls-label:A17695044, umls-label:A18440128, umls-label:A19289777, umls-label:A18444957, umls-label:A17009348, umls-label:A18435393, umls-label:A16992953, umls-label:A19293212, umls-label:A17012085, umls-label:A18444958, umls-label:A17001088, umls-label:A18440129, umls-label:A19284801, umls-label:A19288111