Global Variome shared LOVD

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Phenotype #0000203088 Individual ID 00265290 Associated disease EVR;FEVR Phenotype details nonsyndromic congenital retinal nonattachment (severe subtype of familial exudative vitreoretinopathy; HP:0030490), lack of optic nerve (HP:0008058), leukocoria (HP:0000555) Diagnosis/Initial - Inheritance Familial, autosomal recessive Diagnosis/Definite nonsyndromic congenital retinal nonattachment (NCRNA) Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Jasmine Chen Database submission license No license selected Created by Jasmine Chen Date created 2019-09-19 11:50:56 +02:00 (CEST) Date last edited 2019-09-27 13:47:35 +02:00 (CEST)

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