Phenotype #0000238871

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00315119
Associated disease	kidney disease
Diagnosis/Initial	renal coloboma syndrome
Diagnosis/Definite	-
Phenotype details	Hearing loss; Optic nerve atrophy; Retinal pigment epithelium thinning; abnormal retinal vessels; Nephritis; 60y-renal transplant
Inheritance	Familial
Age/Examination	-
Age/Diagnosis	60y
Age/Onset	19y
Phenotype/Onset	-
Owner name	Matthew Bower
Database submission license	No license selected
Created by	Matthew Bower
Date created	2011-06-21 21:30:23 +02:00 (CEST)
Date last edited	2012-01-13 02:29:39 +01:00 (CET)

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