Phenotype #0000034677

Individual ID 00047405
Associated disease VWD2
Inheritance Familial, autosomal recessive
Diagnosis/Initial -
Disease/Sub-type type 2N
Diagnosis/Definite -
Phenotype details VWF:FVIIIB decreased
Protein VWF_Ag:91, VWF_RCo:51, FVIII_C:10, VWF_CB:85, VWFpp:-
Protein/Multimer_profile hr diffuse;lr ultra-large
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 2015-08-22 13:33:49 +02:00 (CEST)
Date last edited 2016-11-26 17:44:31 +01:00 (CET)

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