Phenotype #0000201818

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00263908
Associated disease	-
Phenotype details	retinitis pigmentosa (HP:0000510), night blindness (HP:0000662), retinal pigment epithelium atrophy (HP:0007791), photophobia (HP:0000613), visual field loss (HP:0007994), posterior subcapsular cataract (HP:0007787)
Diagnosis/Initial	retinitis pigmentosa
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	RP-72
Age/Examination	69y (69 years)
Age/Diagnosis	52y
Age/Onset	30y
Phenotype/Onset	night blindness (HP:0000662)
Protein	-
Owner name	Jasmine Chen
Database submission license	No license selected
Created by	Jasmine Chen
Date created	2019-09-01 17:11:34 +02:00 (CEST)
Date last edited	2019-09-13 12:35:09 +02:00 (CEST)