Phenotype #0000078449

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00100217
Associated disease	VWD2
Inheritance	Familial, autosomal recessive
Diagnosis/Initial	-
Disease/Sub-type	type 2N
Diagnosis/Definite	-
Phenotype details	VWF:FVIIIB decreased
Protein	VWF:Ag 46; VWF:RCo 42; FVIII:C 20
Protein/Multimer_profile	? (unknown; low res);? (unknown; high res)
BleedingScore	-
BleedingScore/Tool	-
Owner name	Daniel J Hampshire
Database submission license
Created by	Daniel J Hampshire
Date created	2017-02-04 12:48:55 +01:00 (CET)
Date last edited	N/A

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