Phenotype #0000045751

Individual ID 00059245
Associated disease VWD2
Inheritance Familial, autosomal dominant
Diagnosis/Initial -
Disease/Sub-type type 2A
Diagnosis/Definite -
Phenotype details 2A(sm); VWF:FVIIIB impaired
Protein VWF_Ag:32, VWF_RCo:23, FVIII_C:25, VWF_CB:15, VWFpp:131
Protein/Multimer_profile hr diffuse;lr relative decrease HMW
BleedingScore 4
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 2016-03-04 16:33:25 +01:00 (CET)
Date last edited 2016-11-26 17:44:31 +01:00 (CET)

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