Phenotype #0000026558

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00033129
Associated disease	-
Phenotype details	onset childhood; retinal degeneration, severe, early onset (EOSRD); Leber congenital amaurosis; tinnitus: BAE normal
Diagnosis/Initial	retinitis pigmentosa
Inheritance	Unknown
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Kornelia Neveling
Database submission license	No license selected
Created by	Kornelia Neveling
Date created	2012-02-04 16:10:11 +01:00 (CET)
Date last edited	2020-08-25 10:48:31 +02:00 (CEST)

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