Phenotype #0000045607

Individual ID 00059019
Associated disease VWD2
Inheritance Familial, autosomal recessive
Diagnosis/Initial -
Disease/Sub-type type 2N
Diagnosis/Definite -
Phenotype details VWF:FVIIIB decreased
Protein VWF_Ag:89, VWF_RCo:74, FVIII_C:10, VWF_CB:-, VWFpp:-
Protein/Multimer_profile hr normal;lr normal
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 2016-02-14 12:54:45 +01:00 (CET)
Date last edited 2016-11-26 17:44:31 +01:00 (CET)

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