Phenotype #0000272859

Individual ID 00377708
Associated disease -
Phenotype details congenital nystagmus, photophobia and were color blind
Diagnosis/Initial retinal dystrophy,autosomal recessive a achromatopsia.
Inheritance Familial, autosomal recessive
Diagnosis/Definite -
Age/Examination 35y (35 years)
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name LOVD
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Julia Lopez
Date created 2021-08-02 20:37:33 +02:00 (CEST)
Date last edited N/A

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