Phenotype #0000020375

Individual ID 00024253
Associated disease VWD2
Inheritance Familial, autosomal recessive
Diagnosis/Initial -
Disease/Sub-type type 2N
Diagnosis/Definite -
Phenotype details VWF:FVIIIB decreased
Protein VWF:Ag 23; VWF:RCo 20; FVIII:C 1.5
Protein/Multimer_profile Absent HMW (low res);? (unknown; high res)
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 2014-11-11 12:36:32 +01:00 (CET)
Date last edited 2019-06-28 14:43:32 +02:00 (CEST)

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