Phenotype #0000039363

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00052786
Associated disease	-
Phenotype details	retinitis pigmentosa; degeneration of the photoreceptors, partial or complete blindness, decreased visual acuity and progressive loss of visual fields
Diagnosis/Initial	retinitis pigmentosa
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Muhammad Ajmal
Database submission license	No license selected
Created by	Muhammad Ajmal
Date created	2015-10-26 17:05:36 +01:00 (CET)
Date last edited	2020-08-25 10:48:31 +02:00 (CEST)

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