Phenotype #0000294765

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00402002
Associated disease	-
Phenotype details	onset early childhood, keratoconus, posterior subcapsular cataract, asteroid hyalosis, reduced color vision
Diagnosis/Initial	retinal degeneration
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Johan den Dunnen
Database submission license
Created by	Johan den Dunnen
Date created	2022-02-03 21:20:11 +01:00 (CET)
Date last edited	N/A

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