Global Variome shared LOVD

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

Phenotype #0000277511 Individual ID 00383726 Associated disease - Phenotype details Total RD, unilateral, OS Diagnosis/Initial persistent fetal vasculature syndrome Inheritance Familial, autosomal dominant Diagnosis/Definite Familial exudative vitreoretinopathy Age/Examination - Age/Diagnosis - Age/Onset 4y Phenotype/Onset - Protein - Owner name LOVD Database submission license Creative Commons Attribution 4.0 International Created by Anna Tracewska Date created 2021-09-29 12:31:11 +02:00 (CEST) Date last edited N/A

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