Phenotype #0000027785

Individual ID 00034389
Associated disease VWD2
Inheritance Familial, autosomal recessive
Diagnosis/Initial -
Disease/Sub-type type 2N
Diagnosis/Definite -
Phenotype details VWF:FVIIIB decreased
Protein VWF_Ag:43, VWF_RCo:49, FVIII_C:7, VWF_CB:-, VWFpp:-
Protein/Multimer_profile lr relative decrease HMW
BleedingScore -
BleedingScore/Tool -
Owner name Daniel J Hampshire
Database submission license Creative Commons Attribution-NonCommercial 4.0 InternationalCreative Commons License
Created by Daniel J Hampshire
Date created 2015-03-17 10:15:23 +01:00 (CET)
Date last edited 2016-11-26 17:44:31 +01:00 (CET)

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