Phenotype #0000310062

Individual ID 00418766
Associated disease neuropathy, optic
Phenotype details -
Diagnosis/Initial -
Diagnosis/Definite -
Inheritance Familial, autosomal dominant
Age/Examination 12y (12 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 11:40:54 +02:00 (CEST)
Date last edited 2023-12-15 11:57:07 +01:00 (CET)

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