Phenotype #0000364285

Individual ID 00479770
Associated disease CORD3
Phenotype details Scotoma, Macular dystrophy, Blurred vision, Color vision defect
Diagnosis/Initial -
Inheritance Familial, autosomal recessive
Diagnosis/Definite -
Age/Examination 18y (18 years)
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Andreas Laner
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Andreas Laner
Date created 2026-05-12 11:20:11 +02:00 (CEST)
Date last edited 2026-05-13 09:57:28 +02:00 (CEST)

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