von Willebrand disease 1
Type 1 von Willebrand disease (type 1 VWD) is a form of VWD characterized by a bleeding disorder associated with a partial quantitative plasmatic deficiency of an otherwise structurally and functionally normal Willebrand factor (von Willebrand factor; VWF). [ Orphanet:166078 ]
Term info
- SCTID:128106003 (MONDO:equivalentTo)
- MESH:D056725 (Orphanet:166078/e)
- NCIT:C131685 (MONDO:equivalentTo)
- DOID:0060573 (MONDO:equivalentTo)
- Orphanet:166078 (OMIM:193400)
- UMLS:C1264039 (Orphanet:166078/e)
- OMIM:193400 (Orphanet:166078/e)
ordo_clinical_subtype
Type 1 von Willebrand disease (type 1 VWD) is a form of VWD characterized by a bleeding disorder associated with a partial quantitative plasmatic deficiency of an otherwise structurally and functionally normal Willebrand factor (von Willebrand factor; VWF).
http://purl.obolibrary.org/obo/Orphanet_166078, http://identifiers.org/mesh/D056725, http://linkedlifedata.com/resource/umls/id/C1264039, https://omim.org/entry/193400, http://purl.obolibrary.org/obo/NCIT_C131685, http://identifiers.org/snomedct/128106003, http://purl.obolibrary.org/obo/DOID_0060573
von Willebrand disease 1, von Willebrand disease type I, VWD1, von Willebrand disease type 1, VWD type 1, von Willebrand's disease type 1, von willebrand's disease 1
VWD, type 1, Von Willebrand disease, type 1, VON WILLEBRAND disease, type 1
MONDO:0008668