Phenotype #0000254783
| Individual ID |
00359530 |
| Associated disease |
OPA1 |
| Phenotype details |
- |
| Diagnosis/Initial |
- |
| Inheritance |
Isolated (sporadic) |
| Diagnosis/Definite |
- |
| Age/Examination |
09y (9 years) |
| Age/Diagnosis |
09y |
| Age/Onset |
- |
| Phenotype/Onset |
- |
| Vision/Acuity |
OD 0.2 LogMAR |
| Vision/Colour |
- |
| Vision/Field |
pericentral |
| Birth_Details |
- |
| Eye/Optic_Disc |
- |
| Eye/OCT |
OS RNFL two or more |
| Brain/Imaging |
normal |
| MotorSkills |
- |
| Vision/Abnormality |
- |
| Hearing/Loss |
- |
| Protein |
- |
| Owner name |
Xingyu Xu |
| Database submission license |
No license selected |
| Created by |
Xingyu Xu |
| Date created |
2021-03-23 18:09:10 +01:00 (CET) |
| Date last edited |
2021-03-24 17:40:41 +01:00 (CET) |
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