Phenotype #0000310047

Individual ID 00418719
Associated disease neuropathy, optic
Phenotype details Abnormal pattern electroretinogram (HP:0030467); Optic atrophy (HP:0000648); Myopia (HP:0000545); Reduced visual acuity (HP:0007663); Abnormal foveal morphology (HP:0000493); Macular dystrophy (HP:0007754)
Diagnosis/Initial -
Diagnosis/Definite -
Inheritance Isolated (sporadic)
Age/Examination 46y (46 years)
Age/Diagnosis -
Age/Onset <18y
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 11:35:49 +02:00 (CEST)
Date last edited 2024-09-09 17:27:56 +02:00 (CEST)

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