Global Variome shared LOVD

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Phenotype #0000272809 Individual ID 00377657 Associated disease - Phenotype details oculomotor apraxia, nystagmus, strabismus, retinal degeneration Diagnosis/Initial Joubert syndrome Inheritance Familial, autosomal recessive Diagnosis/Definite - Age/Examination - 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 2021-08-02 11:30:27 +02:00 (CEST) Date last edited N/A

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