Global Variome shared LOVD

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Phenotype #0000180444 Individual ID 00240379 Associated disease MYOP Phenotype details see paper; ..., neonatal hypotonia, delayed gross motor milestones, mild/moderate obstructive sleep apne Diagnosis/Initial multi-minicore myopathy Inheritance Familial, autosomal recessive Diagnosis/Definite - Age/Examination - 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 2019-06-19 11:55:29 +02:00 (CEST) Date last edited N/A

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