Phenotype #0000173479
| Individual ID |
00230996 |
| Associated disease |
OPA1 |
| Phenotype details |
- |
| Diagnosis/Initial |
- |
| Inheritance |
Familial, autosomal dominant |
| Diagnosis/Definite |
- |
| Age/Examination |
- |
| Age/Diagnosis |
- |
| Age/Onset |
- |
| Phenotype/Onset |
- |
| Vision/Acuity |
- |
| Vision/Colour |
- |
| Vision/Field |
- |
| Birth_Details |
- |
| Eye/Optic_Disc |
- |
| Eye/OCT |
- |
| Brain/Imaging |
- |
| MotorSkills |
- |
| Vision/Abnormality |
- |
| Hearing/Loss |
- |
| Protein |
- |
| Owner name |
Marc Ferre |
| Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
| Created by |
Marc Ferre |
| Date created |
2019-04-22 09:59:18 +02:00 (CEST) |
| Date last edited |
N/A |
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|