Phenotype #0000059718

Individual ID 00080153
Associated disease VWD1
Inheritance Familial, autosomal dominant
Diagnosis/Initial -
Protein VWF_Ag:32, VWF_RCo:38, FVIII_C:115, VWF_CB:33, VWFpp:50
Diagnosis/Definite -
Protein/Multimer_profile hr diffuse;lr normal
BleedingScore 16
BleedingScore/Tool MCMDM-1VWD
Phenotype details -
Owner name Daniel J Hampshire
Database submission license Creative Commons Attribution-NonCommercial 4.0 InternationalCreative Commons License
Created by Daniel J Hampshire
Date created 2016-09-02 11:27:40 +02:00 (CEST)
Date last edited 2016-11-26 18:31:07 +01:00 (CET)

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