Phenotype #0000299657

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00407303
Associated disease	-
Phenotype details	VAOD: 20/100 - VAOS: 20/100, CME OU
Diagnosis/Initial	autosomal dominant retinitis pigmentosa (adRP)
Inheritance	Familial, autosomal dominant
Diagnosis/Definite	-
Age/Examination	13y (13 years)
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	childhood night blindness
Protein	-
Owner name	LOVD
Database submission license
Created by	Julia Lopez
Date created	2022-04-06 13:32:24 +02:00 (CEST)
Date last edited	N/A

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