Global Variome shared LOVD

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

Phenotype #0000242747 Individual ID 00324166 Associated disease CORD5 Phenotype details macular degeneration (HP:0000608), progressive visual loss (HP:0000529), Color vision defect (HP:0000551) Diagnosis/Initial cone-rod dystrophy Inheritance Familial, autosomal dominant Diagnosis/Definite CORD5 Age/Examination 44y (44 years) Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Mariah De Bruin Database submission license No license selected Created by Mariah De Bruin Date created 2020-12-03 11:48:23 +01:00 (CET) Date last edited 2020-12-11 10:05:39 +01:00 (CET)

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.