Phenotype #0000310083

Individual ID 00418786
Associated disease neuropathy, optic
Phenotype details Optic atrophy (HP:0000648); Optic neuropathy (HP:0001138); temporal optic disc pallor (HP:0012511); Color vision defect (HP:0000551); Reduced visual acuity (HP:0007663); Visual field defect (HP:0001123); Abnormality of visual evoked potentials (HP:0000649); Dyschromatopsia (HP:0007641); Red-green dyschromatopsia (HP:0000642)
Diagnosis/Initial -
Diagnosis/Definite -
Inheritance Familial, autosomal dominant
Age/Examination 46y (46 years)
Age/Diagnosis -
Age/Onset 06y
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 18:06:16 +02:00 (CEST)
Date last edited 2023-11-24 13:10:36 +01:00 (CET)

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