Phenotype #0000222592

Individual ID 00288896
Associated disease neuropathy, optic
Phenotype details Peripheral neuropathy (HP:0009830); Ataxia (HP:0001251); Spastic paraparesis (HP:0002313)
Diagnosis/Initial -
Diagnosis/Definite -
Inheritance Familial, autosomal dominant
Age/Examination 67y (67 years)
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Khadidja Guehlouz
Database submission license No license selected
Created by Khadidja Guehlouz
Date created 2020-02-24 20:50:43 +01:00 (CET)
Date last edited 2020-08-25 21:27:59 +02:00 (CEST)

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