Global Variome shared LOVD

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Phenotype #0000272381 Individual ID 00377223 Associated disease - Phenotype details see paper Diagnosis/Initial retinal disease Inheritance Familial, autosomal recessive Diagnosis/Definite achromatopsia, type 3 (ACHM-3) Age/Examination 16y (16 years) Age/Diagnosis 7y Age/Onset 2m Phenotype/Onset - Protein - Owner name LOVD Database submission license Creative Commons Attribution 4.0 International Created by Anna Tracewska Date created 2021-07-16 14:18:12 +02:00 (CEST) Date last edited N/A

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