Phenotype #0000254786
| Individual ID |
00359533 |
| Associated disease |
OPA1 |
| Phenotype details |
- |
| Diagnosis/Initial |
- |
| Inheritance |
Familial, autosomal dominant |
| Diagnosis/Definite |
- |
| Age/Examination |
- |
| Age/Diagnosis |
- |
| Age/Onset |
- |
| Phenotype/Onset |
- |
| Vision/Acuity |
OS 0.6 LogMAR |
| Vision/Colour |
- |
| Vision/Field |
- |
| Birth_Details |
- |
| Eye/Optic_Disc |
- |
| Eye/OCT |
- |
| Brain/Imaging |
- |
| 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 18:36:24 +01:00 (CET) |
| Date last edited |
2021-03-24 17:41:22 +01:00 (CET) |
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