Phenotype #0000275983

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curator: Global Variome, with Curator vacancy

Individual ID	00382141
Associated disease	EVR5
Phenotype details	retinal dystrophy; MIM, 613310 (recessive forms reported)
Diagnosis/Initial	MIM, 613310 (recessive forms reported)
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	LOVD
Database submission license
Created by	Anna Tracewska
Date created	2021-09-07 10:12:12 +02:00 (CEST)
Date last edited	N/A

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