Phenotype #0000280193

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
Register as submitter | Log in

Individual ID	00386385
Associated disease	-
Phenotype details	Night blindness, reduction of the visual field
Diagnosis/Initial	autosomal dominant etinitis pigmentosa
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	Retinitis pigmentosa
Age/Examination	38y (38 years)
Age/Diagnosis	-
Age/Onset	22y
Phenotype/Onset	Night blindness
Protein	-
Owner name	LOVD
Database submission license
Created by	Anna Tracewska
Date created	2021-10-22 11:28:19 +02:00 (CEST)
Date last edited	N/A

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.