Phenotype #0000311011

Individual ID 00419731
Associated disease neuropathy, optic
Phenotype details Optic atrophy (HP:0000648); Optic neuropathy (HP:0001138); Colour vision defect (HP:0000551)
Diagnosis/Initial -
Diagnosis/Definite -
Inheritance Familial, autosomal dominant
Age/Examination 48y (48 years)
Age/Diagnosis -
Age/Onset 07y
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 2022-10-21 16:47:22 +02:00 (CEST)
Date last edited 2023-11-16 11:44:29 +01:00 (CET)

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