Global Variome shared LOVD

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Phenotype #0000277522 Individual ID 00383737 Associated disease - Phenotype details RE retinal fold with peripheral chorioretinal atrophy and pigment LE focal chorioretinopathy Normal MRI brain Diagnosis/Initial Familial exudative vitreoretinopathy associated with microcephaly Inheritance Familial, autosomal dominant Diagnosis/Definite - Age/Examination 14y (14 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 2021-09-29 12:36:52 +02:00 (CEST) Date last edited N/A

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