Phenotype #0000243075

Global Variome shared LOVD

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

Individual ID	00324548
Associated disease	CORD20
Phenotype details	decreased central vision (HP:0007663), dyschromatopsia (HP:0000551) and extreme photophobia (HP:0000613)
Diagnosis/Initial	cone-rod dystrophy
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	CORD20
Age/Examination	61y (61 years)
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Najlae Akhiyate
Database submission license	No license selected
Created by	Najlae Akhiyate
Date created	2020-12-18 12:43:52 +01:00 (CET)
Date last edited	2021-01-05 14:49:29 +01:00 (CET)

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