Global Variome shared LOVD

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Phenotype #0000302148 Individual ID 00410039 Associated disease OPMD Phenotype details clinically definite oculopharyngeal muscular dystrophy, late onset; no retinal dystrophy Diagnosis/Initial - Inheritance Familial, autosomal dominant Diagnosis/Definite oculopharyngeal muscular dystrophy Age/Examination 72y (72 years) Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name LOVD Database submission license Creative Commons Attribution 4.0 International Created by Anna Tracewska Date created 2022-05-18 12:34:52 +02:00 (CEST) Date last edited N/A

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