von Willebrand disease 2
von Willebrand disease type 2M
UMLS:C1282974
NCIT:C131688
Editor note: 2 sctitds refer to same disease
MONDO:0015630
Orphanet:166090
SCTID:359725000
SCTID:359729006
GARD:17023
von Willebrand disease, type 2M
A subtype of type 2 VWD characterized by a bleeding disorder associated with a decrease in the affinity of the Willebrand factor (von Willebrand factor; VWF) for platelets and the subendothelium in the absence of any deficiency of high molecular weight VWF multimers.