Phenotype #0000058775

Individual ID 00079020
Associated disease VWD2
Inheritance Familial, autosomal dominant
Diagnosis/Initial -
Disease/Sub-type type 2A
Diagnosis/Definite -
Phenotype details 2A(IIE); VWF:FVIIIB normal
Protein VWF_Ag:42, VWF_RCo:13, FVIII_C:78, VWF_CB:24, VWFpp:134
Protein/Multimer_profile hr diffuse;lr relative decrease HMW
BleedingScore 10
BleedingScore/Tool MCMDM-1VWD
Owner name Daniel J Hampshire
Database submission license Creative Commons Attribution-NonCommercial 4.0 InternationalCreative Commons License
Created by Daniel J Hampshire
Date created 2016-07-29 18:03:34 +02:00 (CEST)
Date last edited 2016-11-26 17:44:31 +01:00 (CET)

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