Phenotype #0000081208

Individual ID 00103077
Associated disease VWD2
Inheritance Familial, autosomal dominant
Diagnosis/Initial -
Disease/Sub-type type 2A
Diagnosis/Definite -
Phenotype details -
Protein VWF:Ag 13; VWF:RCo 12; FVIII:C 15
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 2017-04-04 11:12:58 +02:00 (CEST)
Date last edited N/A

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