Phenotype #0000059746

Individual ID 00080183
Associated disease VWD1
Inheritance Familial, autosomal dominant
Diagnosis/Initial -
Protein VWF_Ag:36, VWF_RCo:28, FVIII_C:39, VWF_CB:20, VWFpp:84
Diagnosis/Definite -
Protein/Multimer_profile hr diffuse;lr relative decrease HMW
BleedingScore 9
BleedingScore/Tool MCMDM-1VWD
Phenotype details VWF:FVIIIB moderately decreased
Owner name Daniel J Hampshire
Database submission license Creative Commons Attribution-NonCommercial 4.0 InternationalCreative Commons License
Created by Daniel J Hampshire
Date created 2016-09-02 16:44:34 +02:00 (CEST)
Date last edited 2016-11-26 18:31:07 +01:00 (CET)

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
  Powered by LOVD v.3.0 Build 30b
LOVD software ©2004-2024 Leiden University Medical Center
Database contents © by their respective submitters and curators
 There are currently no updates.