A heart conduction disease characterized by orthostatic intolerance that has_material_basis_in heterozygous mutation in the SLC6A2 gene on chromosome 16q12.2.
synonyms:
ORDO:443236,
ICD10CM:I95.1,
irritable heart,
mitral valve prolapse syndrome,
orthostatic intolerance due to NET deficiency,
orhtostatic intolerance,
OMIM:604715,
familial orthostatic tachycardia due to norepinephrine transporter deficiency,
postural tachycardia syndrome due to NET deficiency,
