Phenotype #0000045750

Individual ID 00059244
Associated disease VWD1
Inheritance Familial, autosomal dominant
Diagnosis/Initial -
Protein VWF:Ag 47; VWF:RCo 38; FVIII:C 40; VWF:CB 59; VWFpp 105
Diagnosis/Definite -
Protein/Multimer_profile Normal (low res);Normal satellite bands (high res)
BleedingScore 7
BleedingScore/Tool MCMDM-1VWD
Phenotype details VWF:FVIIIB impaired
Owner name Daniel J Hampshire
Database submission license Creative Commons Attribution-NonCommercial 4.0 InternationalCreative Commons License
Created by Daniel J Hampshire
Date created 2016-03-04 15:53:19 +01:00 (CET)
Date last edited 2019-05-20 15:43:22 +02:00 (CEST)

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