Phenotype #0000045749

Individual ID 00059243
Associated disease VWD1
Inheritance Familial, autosomal dominant
Diagnosis/Initial -
Protein VWF:Ag 37; VWF:RCo 32; FVIII:C 28; VWF:CB 43; VWFpp 67
Diagnosis/Definite -
Protein/Multimer_profile Normal (low res);Normal satellite bands (high res)
BleedingScore 2
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 15:29:27 +01:00 (CET)
Date last edited 2019-06-04 14:57:53 +02:00 (CEST)

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