Phenotype #0000015398

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00017034
Associated disease	NPHP1
Phenotype details	severe renal involvement progressing to ESRD <5y; speech delay, hydrocephalus; age ESDR 4,5y
Diagnosis/Initial	-
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	-
Age/Examination	?
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Marianne Vos (LOVD-team)
Database submission license	No license selected
Created by	Marianne Vos (LOVD-team)
Date created	2014-06-14 11:09:22 +02:00 (CEST)
Date last edited	2016-06-19 17:35:25 +02:00 (CEST)

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