Phenotype #0000157477

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curators: Zoe Baily, Marion MacFarlane, and Raymond Dalgleish

Individual ID	00208868
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	2018-12-19 02:16:00 +01:00 (CET)
Date last edited	2019-03-03 11:47:38 +01:00 (CET)

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