Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ] Register as submitter | Log in

Phenotype #0000157471 Individual ID 00208862 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 00:52:05 +01:00 (CET) Date last edited 2018-12-20 09:35:56 +01:00 (CET)

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