Phenotype #0000310060

Individual ID 00418764
Associated disease neuropathy, optic
Phenotype details Color vision defect (HP:0000551); Abnormality of visual evoked potentials (HP:0000649); Abnormal electroretinogram (HP:0000512)
Diagnosis/Initial -
Diagnosis/Definite -
Inheritance Familial, autosomal dominant
Age/Examination 51y (51 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 2022-10-06 11:21:03 +02:00 (CEST)
Date last edited 2024-03-17 12:16:44 +01:00 (CET)

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