Global Variome shared LOVD

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Phenotype #0000308411 Individual ID 00416899 Associated disease EVR2 Phenotype details 0m: retina: avascular temporal peripheries and vascular shunts at the site of the joining of the vascularized and avascularized tissue similar to that observed in retinopathy of prematurity; treated with cryotherapy, maintained their sight; myopia Diagnosis/Initial - Inheritance Familial, X-linked recessive Diagnosis/Definite familial exudative vitreoretinopathy Age/Examination 11y (11 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 2022-09-09 15:34:26 +02:00 (CEST) Date last edited N/A

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