Phenotype #0000291708

Individual ID 00398621
Associated disease -
Phenotype details total color blindness; severe photophobia and nystagmus
Diagnosis/Initial -
Inheritance Familial, autosomal recessive
Diagnosis/Definite achromatopsia
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name LOVD
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Anna Tracewska
Date created 2022-01-07 12:22:23 +01:00 (CET)
Date last edited N/A

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