Phenotype #0000243075

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)

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