Phenotype #0000058631
| Individual ID |
00078872 |
| Associated disease |
LGMDR12;LGMD2L |
| Phenotype details |
- |
| Diagnosis/Initial |
- |
| Inheritance |
Familial, autosomal dominant |
| Diagnosis/Definite |
- |
| Age/Examination |
- |
| Age/Diagnosis |
- |
| Age/Onset |
- |
| Phenotype/Onset |
- |
| Protein |
- |
| Owner name |
Tom Winder |
| Database submission license |
No license selected |
| Created by |
Tom Winder |
| Date created |
2013-06-28 23:10:26 +02:00 (CEST) |
| Date last edited |
2013-06-29 20:56:42 +02:00 (CEST) |
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|