Phenotype #0000157465

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	00208856
Associated disease	LCA2
Phenotype details	poor vision, onset as infant, flat ERG
Diagnosis/Initial	-
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Bailey Glen
Database submission license	No license selected
Created by	Bailey Glen
Date created	2018-12-18 23:38:53 +01:00 (CET)
Date last edited	2019-03-03 11:47:38 +01:00 (CET)

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