Phenotype #0000066755

Individual ID 00087228
Associated disease VWD2
Inheritance Familial, autosomal recessive
Diagnosis/Initial -
Disease/Sub-type type 2N
Diagnosis/Definite -
Phenotype details VWF:FVIIIB severely decreased
Protein VWF:Ag 79; VWF:RCo 81; FVIII:C 8
Protein/Multimer_profile Normal (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 2016-11-16 13:29:52 +01:00 (CET)
Date last edited 2019-06-27 12:33:06 +02:00 (CEST)

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