Phenotype #0000310084

Individual ID 00418787
Associated disease neuropathy, optic
Phenotype details Optic atrophy (HP:0000648); Optic neuropathy (HP:0001138); temporal optic disc pallor (HP:0012511); Reduced visual acuity (HP:0007663); Abnormality of visual evoked potentials (HP:0000649); Visual field defect (HP:0001123); Myopia (HP:0000545); Macular schisis (HP:0011511)
Diagnosis/Initial -
Diagnosis/Definite -
Inheritance Familial, autosomal dominant
Age/Examination 50y (50 years)
Age/Diagnosis -
Age/Onset 30y
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 2022-10-06 18:35:39 +02:00 (CEST)
Date last edited 2024-09-09 17:28:22 +02:00 (CEST)

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