Global Variome shared LOVD

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Phenotype #0000058777 Individual ID 00079022 Associated disease VWD1 Inheritance Familial, autosomal dominant Diagnosis/Initial - Protein VWF:Ag 11; VWF:RCo 7; FVIII:C 18; VWF:CB 6; VWFpp 127 Diagnosis/Definite - Protein/Multimer_profile Normal (low res);Normal satellite bands (high res) BleedingScore 18 BleedingScore/Tool MCMDM-1VWD Phenotype details VWF:FVIIIB normal Owner name Daniel J Hampshire Database submission license Creative Commons Attribution-NonCommercial 4.0 International Created by Daniel J Hampshire Date created 2016-07-29 19:01:00 +02:00 (CEST) Date last edited 2017-04-20 13:43:03 +02:00 (CEST)

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