Global Variome shared LOVD

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Phenotype #0000034675 Individual ID 00047403 Associated disease VWD2 Inheritance Familial, autosomal recessive Diagnosis/Initial - Disease/Sub-type type 2N Diagnosis/Definite - Phenotype details VWF:FVIIIB decreased Protein VWF_Ag:65, VWF_RCo:70, FVIII_C:6, VWF_CB:-, VWFpp:- Protein/Multimer_profile lr normal BleedingScore - BleedingScore/Tool - Owner name Daniel J Hampshire Database submission license Creative Commons Attribution-NonCommercial 4.0 International Created by Daniel J Hampshire Date created 2015-08-22 13:01:56 +02:00 (CEST) Date last edited 2016-11-26 17:44:31 +01:00 (CET)

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