Phenotype #0000020386

Individual ID 00024267
Associated disease VWD1
Inheritance Familial, autosomal dominant
Diagnosis/Initial -
Protein VWF_Ag:38, VWF_RCo:29, FVIII_C:55, VWF_CB:22, VWFpp:57
Diagnosis/Definite -
Protein/Multimer_profile hr normal;lr normal
BleedingScore 6
BleedingScore/Tool MCMDM-1VWD
Phenotype details -
Owner name Daniel J Hampshire
Database submission license Creative Commons Attribution-NonCommercial 4.0 InternationalCreative Commons License
Created by Daniel J Hampshire
Date created 2014-11-13 16:24:47 +01:00 (CET)
Date last edited 2016-11-26 18:31:07 +01:00 (CET)

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