Global Variome shared LOVD

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Phenotype #0000302144 Individual ID 00410035 Associated disease - Phenotype details oculopharyngeal muscular dystrophy, early onset Diagnosis/Initial - Inheritance Unknown Diagnosis/Definite retinal dystrophy and oculopharyngeal muscular dystrophy Age/Examination 35y (35 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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