Global Variome shared LOVD

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

Phenotype #0000325414 Individual ID 00435214 Associated disease LCA6 Phenotype details - Diagnosis/Initial Leber congenital amaurosis Inheritance Familial, autosomal recessive Diagnosis/Definite LCA6 Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Kaoruko Torii Database submission license Creative Commons Attribution 4.0 International Created by Kaoruko Torii Date created 2023-06-12 11:33:28 +02:00 (CEST) Date last edited 2023-06-12 14:49:05 +02:00 (CEST)

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