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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