Phenotype #0000311185

Individual ID 00419916
Associated disease neuropathy, optic
Phenotype details Optic atrophy (HP:0000648); Optic neuropathy (HP:0001138); Nephropathy (HP:0000112); Reduced visual acuity (HP:0007663); Chronic kidney disease (HP:0012622)
Diagnosis/Initial -
Diagnosis/Definite -
Inheritance Familial, autosomal dominant
Age/Examination 25y (25 years)
Age/Diagnosis -
Age/Onset ?
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 2022-10-25 14:42:36 +02:00 (CEST)
Date last edited 2024-09-14 14:56:25 +02:00 (CEST)

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