Phenotype #0000317598

Individual ID 00426444
Associated disease -
Phenotype details onset of night blindness: childhood; best corrected visual acuity right/left eye: no light perception/no light perception; cataract; fundus appearance: not available; visual field: not available; electroretinogram: not available
Diagnosis/Initial -
Inheritance Familial, autosomal dominant
Diagnosis/Definite retinitis pigmentosa
Age/Examination 71y (71 years)
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 2022-11-30 12:31:10 +01:00 (CET)
Date last edited N/A

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