Global Variome shared LOVD

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

Phenotype #0000027034 Individual ID 00033605 Associated disease CORD Inheritance Familial, autosomal recessive Diagnosis/Initial - Age/Examination - Diagnosis/Definite - Age/Diagnosis - Age/Onset - Phenotype/Onset - Phenotype details Cone-rod dystrophy with nystagmus Protein - Owner name Marcel Nelen Database submission license No license selected Created by Marcel Nelen Date created 2013-10-02 09:46:06 +02:00 (CEST) Date last edited N/A

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