Phenotype #0000299758
| Individual ID |
00407589 |
| Associated disease |
- |
| Phenotype details |
13y: best corrected visual acuity right, left eye: 20/200, 20/200, refraction (spherical equivalent): +4, electroretinogram: not detectable, renal disease: none |
| Diagnosis/Initial |
- |
| Inheritance |
Familial, autosomal recessive |
| Diagnosis/Definite |
Leber congenital amaurosis |
| Age/Examination |
- |
| Age/Diagnosis |
- |
| Age/Onset |
- |
| Phenotype/Onset |
- |
| Protein |
- |
| Owner name |
LOVD |
| Database submission license |
Creative Commons Attribution 4.0 International |
| Created by |
Anna Tracewska |
| Date created |
2022-04-06 19:14:38 +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.
|