Phenotype #0000238828

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curator: Global Variome, with Curator vacancy

Individual ID	00315076
Associated disease	kidney disease
Diagnosis/Initial	renal hypolasia
Diagnosis/Definite	-
Phenotype details	no eye anomalies; Renal hypodysplasia-bilateral
Inheritance	Familial
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Owner name	Matthew Bower
Database submission license	No license selected
Created by	Matthew Bower
Date created	2011-06-20 17:02:09 +02:00 (CEST)
Date last edited	2011-06-29 14:28:13 +02:00 (CEST)

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