Phenotype #0000086997
| Individual ID |
00109972 |
| Associated disease |
AT |
| Phenotype details |
Affected sister (14686) and affected male cousin (10-0375) homozygous for the same variant |
| Diagnosis/Initial |
- |
| Inheritance |
Unknown |
| Diagnosis/Definite |
- |
| Age/Examination |
- |
| Age/Diagnosis |
- |
| Age/Onset |
- |
| Phenotype/Onset |
- |
| Protein |
- |
| Owner name |
Patrick Concannon |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Patrick Concannon |
| Date created |
2012-01-05 20:50:58 +01:00 (CET) |
| Date last edited |
2012-01-05 20:54:41 +01:00 (CET) |
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|