Global Variome shared LOVD

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Phenotype #0000291707 Individual ID 00398620 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 International Created by Anna Tracewska Date created 2022-01-07 12:22:23 +01:00 (CET) Date last edited N/A

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