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 International |
| 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) |
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|