Phenotype #0000201769

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00263407
Associated disease	-
Phenotype details	retinitis pigmentosa (HP:0000510), night blindness (HP:0000662), chorioretinal atrophy (HP:0000533)
Diagnosis/Initial	retinitis pigmentosa
Inheritance	Familial
Diagnosis/Definite	retinitis pigmentosa
Age/Examination	-
Age/Diagnosis	-
Age/Onset	47y
Phenotype/Onset	night blindness (HP:0000662)
Protein	-
Owner name	Jasmine Chen
Database submission license	No license selected
Created by	Jasmine Chen
Date created	2019-08-27 11:13:25 +02:00 (CEST)
Date last edited	2020-08-25 10:48:31 +02:00 (CEST)

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