Phenotype #0000123787

Individual ID 00151393
Associated disease VWD2
Inheritance Familial, autosomal dominant
Diagnosis/Initial -
Disease/Sub-type type 2A
Diagnosis/Definite -
Phenotype details -
Protein VWF:Ag 30; VWF:RCo <5; FVIII:C 20
Protein/Multimer_profile Absent HMW (low res);? (unknown; high res)
BleedingScore -
BleedingScore/Tool -
Owner name Daniel J Hampshire
Database submission license Creative Commons Attribution-NonCommercial 4.0 InternationalCreative Commons License
Created by Daniel J Hampshire
Date created 2018-01-16 11:19:49 +01:00 (CET)
Date last edited N/A

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