Phenotype #0000058777

Individual ID 00079022
Associated disease VWD1
Inheritance Familial, autosomal dominant
Diagnosis/Initial -
Protein VWF:Ag 11; VWF:RCo 7; FVIII:C 18; VWF:CB 6; VWFpp 127
Diagnosis/Definite -
Protein/Multimer_profile Normal (low res);Normal satellite bands (high res)
BleedingScore 18
BleedingScore/Tool MCMDM-1VWD
Phenotype details VWF:FVIIIB normal
Owner name Daniel J Hampshire
Database submission license Creative Commons Attribution-NonCommercial 4.0 InternationalCreative Commons License
Created by Daniel J Hampshire
Date created 2016-07-29 19:01:00 +02:00 (CEST)
Date last edited 2017-04-20 13:43:03 +02:00 (CEST)

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