Global Variome shared LOVD

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Phenotype #0000039101 Individual ID 00052524 Associated disease LCA Phenotype details Leber congenital amaurosis; night blindness, pigmentary stippling of retina, early pigment migration, attenuated vessels, hypopigmentation of macula, flat ERG, esotropia, constriction in visual field Diagnosis/Initial - Inheritance Familial, autosomal recessive Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset 3m Phenotype/Onset - Protein - Owner name Muhammad Ajmal Database submission license No license selected Created by Muhammad Ajmal Date created 2015-10-26 17:05:36 +01:00 (CET) Date last edited N/A

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