Phenotype #0000027190
| Individual ID |
00033792 |
| Associated disease |
FHCL2 |
| Phenotype details |
- |
| Diagnosis/Initial |
- |
| Inheritance |
Familial, autosomal dominant |
| Diagnosis/Definite |
- |
| Age/Examination |
- |
| Age/Diagnosis |
- |
| Age/Onset |
- |
| Phenotype/Onset |
- |
| Protein |
- |
| Owner name |
Ingrid Braenne |
| Database submission license |
No license selected |
| Created by |
Ingrid Braenne |
| Date created |
2015-03-05 10:10:53 +01:00 (CET) |
| Date last edited |
2016-02-13 03:23:54 +01:00 (CET) |
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|