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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