Global Variome shared LOVD

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

Phenotype #0000055858 Individual ID 00076083 Associated disease CORD Inheritance Familial, autosomal recessive Diagnosis/Initial - Age/Examination - Diagnosis/Definite - Age/Diagnosis - Age/Onset 12y Phenotype/Onset unknown Phenotype details cone-rod dystrophy (HP:0000510); Reduced cone and rod ERGs, OD: CF, OS: CF, Widely extinguished visual field with remaining peripheral island, Severe panretinal atrophy Protein - Owner name Stéphanie Cornelis Database submission license Creative Commons Attribution 4.0 International Created by Stéphanie Cornelis Date created 2016-02-22 12:22:09 +01:00 (CET) Date last edited N/A

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