Phenotype #0000129665

Individual ID 00164628
Associated disease HOKPP
Phenotype details -
Diagnosis/Initial hypokalaemic periodic paralyses
Inheritance Familial, autosomal dominant
Diagnosis/Definite hypokalaemic periodic paralyses
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Emil Gustavsson
Database submission license No license selected
Created by Emil Gustavsson