Global Variome shared LOVD

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

Phenotype #0000242875 Individual ID 00324332 Associated disease CORD5 Phenotype details Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608 Diagnosis/Initial cone-rod dystrophy Inheritance Familial, autosomal dominant Diagnosis/Definite CORD5 Age/Examination 28y (28 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 2020-12-07 11:48:03 +01:00 (CET) Date last edited 2020-12-11 10:05:39 +01:00 (CET)

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