Phenotype #0000250172

Individual ID 00331981
Associated disease -
Phenotype details night vision problems; scotopic ERG normalreduced; photopic ERG borderline
Diagnosis/Initial macular dystrophy or cone-rod dystrophy
Inheritance Familial, autosomal recessive
Diagnosis/Definite -
Age/Examination 57y (57 years)
Age/Diagnosis -
Age/Onset -
Phenotype/Onset night vision problems
Protein -
Owner name LOVD
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2021-02-14 10:12:05 +01:00 (CET)
Date last edited N/A

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