Phenotype #0000123935

Individual ID 00151564
Associated disease VWD2
Inheritance Familial, autosomal dominant
Diagnosis/Initial -
Disease/Sub-type type 2B
Diagnosis/Definite -
Phenotype details -
Protein VWF:Ag 85; VWF:RCo 40; FVIII:C 71
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 2018-01-20 16:06:19 +01:00 (CET)
Date last edited N/A

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