Phenotype #0000276717

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00382861
Associated disease	-
Phenotype details	moderate disease; night blindness 31y; marked atrophy of the peripheral retina
Diagnosis/Initial	retinitis pigmentosa (RP)
Inheritance	Familial, autosomal dominant
Diagnosis/Definite	-
Age/Examination	30y (30 years)
Age/Diagnosis	-
Age/Onset	30y
Phenotype/Onset	-
Protein	-
Owner name	LOVD
Database submission license
Created by	Julia Lopez
Date created	2021-09-13 01:01:20 +02:00 (CEST)
Date last edited	N/A

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