Global Variome shared LOVD

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Phenotype #0000059746 Individual ID 00080183 Associated disease VWD1 Inheritance Familial, autosomal dominant Diagnosis/Initial - Protein VWF_Ag:36, VWF_RCo:28, FVIII_C:39, VWF_CB:20, VWFpp:84 Diagnosis/Definite - Protein/Multimer_profile hr diffuse;lr relative decrease HMW BleedingScore 9 BleedingScore/Tool MCMDM-1VWD Phenotype details VWF:FVIIIB moderately decreased Owner name Daniel J Hampshire Database submission license Creative Commons Attribution-NonCommercial 4.0 International Created by Daniel J Hampshire Date created 2016-09-02 16:44:34 +02:00 (CEST) Date last edited 2016-11-26 18:31:07 +01:00 (CET)

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