Phenotype #0000027789

Individual ID 00034393
Associated disease VWD1
Inheritance Familial, autosomal dominant
Diagnosis/Initial -
Protein VWF:Ag 59; VWF:RCo 44; FVIII:C 9; VWF:CB 38; VWFpp 76
Diagnosis/Definite -
Protein/Multimer_profile Normal (low res);Normal satellite bands (high res)
BleedingScore 6
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 2015-03-17 12:51:58 +01:00 (CET)
Date last edited 2017-02-03 13:10:02 +01:00 (CET)

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