Phenotype #0000316139

Individual ID 00424940
Associated disease RP
Diagnosis/Initial retinitis pigmentosa
Diagnosis/Definite -
Phenotype details decreased night vision, followed by peripheral visual field loss; retinitis pigmentosa, myopic astigmatism, left eye cystoid macular oedema; hearing impairment
Inheritance Familial, autosomal recessive
Age/Examination 30y (30 years)
Age/Diagnosis -
Age/Onset 10y
Phenotype/Onset -
Protein -
Owner name Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2022-11-23 16:47:05 +01:00 (CET)
Date last edited N/A

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