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) |
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