Global Variome shared LOVD

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Phenotype #0000360750 Individual ID 00476076 Associated disease MYOP Diagnosis/Initial congenital myopathy Diagnosis/Definite - Phenotype details details not specified; ncorrelation clinical diagnosis with genetic diagnosis Inheritance Familial, autosomal recessive Age/Examination 6y (6 years) Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2026-04-13 18:16:22 +02:00 (CEST) Date last edited N/A

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