Phenotype #0000034660

Individual ID 00047303
Associated disease VWD2
Inheritance Familial, autosomal recessive
Diagnosis/Initial -
Disease/Sub-type type 2N
Diagnosis/Definite -
Phenotype details VWF:FVIIIB decreased
Protein VWF:Ag 76; VWF:RCo 71; FVIII:C 17
Protein/Multimer_profile Ultra-large (low res);Diffuse satellite bands (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 2015-08-15 14:08:01 +02:00 (CEST)
Date last edited 2019-06-27 12:10:41 +02:00 (CEST)

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