Phenotype #0000045737

Individual ID 00059231
Associated disease VWD2
Inheritance Familial, autosomal recessive
Diagnosis/Initial -
Disease/Sub-type type 2N
Diagnosis/Definite -
Phenotype details -
Protein VWF_Ag:86, VWF_RCo:103, FVIII_C:43, VWF_CB:-, VWFpp:-
Protein/Multimer_profile lr normal
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 2016-03-04 10:43:56 +01:00 (CET)
Date last edited 2016-11-26 17:44:31 +01:00 (CET)

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