Global Variome shared LOVD

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Phenotype #0000292472 Individual ID 00399357 Associated disease FVH2 Phenotype details see paper; ..., foveal hypoplasia, optic nerve misrouting, Kartagener syndrome Diagnosis/Initial foveal hypoplasia, Kartagener syndrome Inheritance Familial, autosomal recessive Diagnosis/Definite FVH2 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 2022-01-19 20:50:47 +01:00 (CET) Date last edited N/A

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