Phenotype #0000144093

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00183357
Associated disease	-
Phenotype details	central chorioretinal atrophy, peripheral reticular dystrophy, sensorineural hearing loss (adult onset), ...
Diagnosis/Initial	retinitis pigmentosa
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	RDEOA
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Johan den Dunnen
Database submission license
Created by	Johan den Dunnen
Date created	2018-10-23 18:59:49 +02:00 (CEST)
Date last edited	N/A

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