Global Variome shared LOVD

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

Phenotype #0000288001 Individual ID 00394801 Associated disease - Phenotype details corneal dystrophy and concomitant retinal pigmentary degeneration Diagnosis/Initial - Inheritance Familial, autosomal dominant Diagnosis/Definite inherited retinal disease Age/Examination 17y (17 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 2021-12-02 12:05:39 +01:00 (CET) Date last edited N/A

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