Phenotype #0000310052

Individual ID 00418756
Associated disease neuropathy, optic
Phenotype details Nyctalopia (HP:0000662); Retinal dystrophy (HP:0000556); Retinal pigment epithelial atrophy (HP:0007722); Photoreceptor layer loss on macular OCT (HP:0030609); Reduced visual acuity (HP:0007663)
Diagnosis/Initial -
Diagnosis/Definite -
Inheritance Unknown
Age/Examination ?
Age/Diagnosis -
Age/Onset 59y
Phenotype/Onset -
Protein -
Owner name Mohamed Selhane
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Mohamed Selhane
Date created 2022-10-05 18:00:24 +02:00 (CEST)
Date last edited 2024-09-09 17:28:15 +02:00 (CEST)

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