Phenotype #0000015237

Individual ID	00016584
Associated disease	RD
Phenotype details	more severe phenotype with poor vision from the first years of life, severe generalized cone-system dysfunction, and additional significant involvement of rod photoreceptors.
Diagnosis/Initial	-
Inheritance	Isolated (sporadic)
Diagnosis/Definite	-
Age/Examination	>46y (later than 46 years)
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Marianne Vos (LOVD-team)
Database submission license	No license selected
Created by	Johan den Dunnen
Date created	2014-05-28 20:51:15 +02:00 (CEST)
Date last edited	2014-05-28 20:52:03 +02:00 (CEST)

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