Phenotype #0000017689

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00018452
Associated disease	NPHS
Phenotype details	congenital nephrotic syndrome, haematuria
Diagnosis/Initial	-
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Elisabet Ars Criach
Database submission license	No license selected
Created by	Elisabet Ars Criach
Date created	2014-09-18 10:09:19 +02:00 (CEST)
Date last edited	2018-02-16 15:21:48 +01:00 (CET)

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