Phenotype #0000254824
Individual ID |
00359571 |
Associated disease |
OPA1 |
Phenotype details |
- |
Diagnosis/Initial |
Optic atrophy |
Inheritance |
Familial, autosomal dominant |
Diagnosis/Definite |
- |
Age/Examination |
12y (12 years) |
Age/Diagnosis |
- |
Age/Onset |
- |
Phenotype/Onset |
- |
Vision/Acuity |
OS 0.4 LogMAR |
Vision/Colour |
- |
Vision/Field |
- |
Birth_Details |
- |
Eye/Optic_Disc |
- |
Eye/OCT |
OS RNFL two or more |
Brain/Imaging |
- |
MotorSkills |
- |
Vision/Abnormality |
- |
Hearing/Loss |
- |
Protein |
- |
Owner name |
Xingyu Xu |
Database submission license |
No license selected |
Created by |
Xingyu Xu |
Date created |
2021-03-26 09:30:58 +01:00 (CET) |
Date last edited |
2021-03-26 11:02:06 +01:00 (CET) |
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