Phenotype #0000127732

Individual ID 00155000
Associated disease VWD2
Inheritance Familial, autosomal dominant
Diagnosis/Initial -
Disease/Sub-type type 2B
Diagnosis/Definite -
Phenotype details -
Protein VWF:Ag 68; VWF:RCo 14; FVIII:C 39
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 2018-03-08 15:28:35 +01:00 (CET)
Date last edited 2019-07-19 12:16:53 +02:00 (CEST)

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