Phenotype #0000015257
| Individual ID |
00016855 |
| Associated disease |
MYMY6 |
| Phenotype details |
Achalasia; No extra digestive investigation was realized in F3 IV-2, F3 IV-4, or F3 IV-5 in the absence of neurological symptoms. |
| Diagnosis/Initial |
- |
| Inheritance |
Familial, autosomal recessive |
| Diagnosis/Definite |
- |
| Age/Examination |
23y (23 years) |
| Age/Diagnosis |
- |
| Age/Onset |
- |
| Phenotype/Onset |
- |
| Protein |
- |
| Owner name |
Marianne Vos (LOVD-team) |
| Database submission license |
No license selected |
| Created by |
Marianne Vos (LOVD-team) |
| Date created |
2014-06-03 18:14:58 +02:00 (CEST) |
| Date last edited |
2016-06-19 09:58:44 +02:00 (CEST) |
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|