Phenotype #0000207736

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00269941
Associated disease	-
Phenotype details	pericentral RP, incidental diagnosis; hearing loss, constricted with ring scotoma, pseudophakic
Diagnosis/Initial	retinitis pigmentosa
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	-
Age/Examination	47y (47 years)
Age/Diagnosis	-
Age/Onset	11y
Phenotype/Onset	-
Protein	-
Owner name	Sandro Banfi
Database submission license	No license selected
Created by	Sandro Banfi
Date created	2019-12-10 15:17:30 +01:00 (CET)
Date last edited	2020-08-25 10:48:31 +02:00 (CEST)

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