Phenotype #0000127668
| Individual ID |
00154933 |
| Associated disease |
SCA5 |
| Inheritance |
Isolated (sporadic) |
| Diagnosis/Initial |
- |
| Age/Examination |
- |
| Diagnosis/Definite |
- |
| Age/Diagnosis |
01y11m |
| Age/Onset |
- |
| Phenotype/Onset |
Cerebellar atrophy, cerebellar ataxia, developmental delay, strabismus, dolicocephaly |
| Phenotype details |
- |
| Protein |
- |
| Owner name |
Enza Maria Valente |
| Database submission license |
No license selected |
| Created by |
Enza Maria Valente |
| Date created |
2018-03-05 14:20:52 +01:00 (CET) |
| Date last edited |
2020-01-24 15:28:35 +01:00 (CET) |
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|