Global Variome shared LOVD

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Phenotype #0000187805 Individual ID 00248836 Associated disease CORD Inheritance Familial, autosomal recessive Diagnosis/Initial cone-rod dystrophy Age/Examination - Diagnosis/Definite - Age/Diagnosis - Age/Onset - Phenotype/Onset - Phenotype details see paper; ..., isolated cone-rod dystrophy, skeletal involvement Protein - Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2019-07-28 14:21:35 +02:00 (CEST) Date last edited N/A

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