Phenotype #0000307600

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00415828
Associated disease	-
Phenotype details	detailed clinical description of a subset of these patients has been presented in {PMID:Michaelides 2005:15722315}
Diagnosis/Initial	-
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	cone dystrophy with supernormal rod electroretinogram
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	LOVD
Database submission license
Created by	Anna Tracewska
Date created	2022-08-17 09:35:59 +02:00 (CEST)
Date last edited	N/A

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