Global Variome shared LOVD

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Phenotype #0000237152 Individual ID 00312023 Associated disease neuropathy, optic Phenotype details Reduced visual acuity (HP:0007663); Optic atrophy (HP:0000648); Dyschromatopsia (HP:0007641); Global developmental delay (HP:0001263) Diagnosis/Initial - Diagnosis/Definite - Inheritance Isolated (sporadic) Age/Examination 07y (7 years) Age/Diagnosis - Age/Onset ? Phenotype/Onset - Protein - Owner name Benjamin Billiet Database submission license No license selected Created by Benjamin Billiet Date created 2020-09-30 10:49:08 +02:00 (CEST) Date last edited 2021-05-05 16:34:12 +02:00 (CEST)

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