Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ] Register as submitter | Log in

Phenotype #0000207933 Individual ID 00271323 Associated disease EVR;FEVR Phenotype details unilateral congenital visual loss (HP:0030553), persistent hyperplasia primary vitreous (HP:0007968) Diagnosis/Initial - Inheritance Familial Diagnosis/Definite persistent hyperplasia primary vitreous Age/Examination 19y (19 years) Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Jasmine Chen Database submission license No license selected Created by Jasmine Chen Date created 2019-12-18 00:48:22 +01:00 (CET) Date last edited 2020-01-10 09:43:05 +01:00 (CET)

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