Clinical and research tests for Potassium thiocyanate-13C - Genetic Testing Registry (GTR)

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Select all conditions on this page	Conditions	Synonyms
Select item 41523	Type 2 diabetes mellitus Tests Genes GeneReviews	DIABETES MELLITUS, TYPE 2, PROTECTION AGAINST Diabetes mellitus, noninsulin-dependent, late onset KCNJ11-Related Susceptibility to Noninsulin-Dependent Diabetes Mellitus Type II diabetes mellitus
Select item 318554	Episodic ataxia type 1 Tests Gene GeneReviews	ATAXIA, EPISODIC, WITH MYOKYMIA Episodic ataxia/myokymia syndrome MYOKYMIA WITH PERIODIC ATAXIA PAROXYSMAL ATAXIA WITH NEUROMYOTONIA, HEREDITARY
Select item 2562	Beckwith-Wiedemann syndrome Tests Genes GeneReviews	EMG Syndrome Exomphalos macroglossia gigantism syndrome
Select item 82890	Pendred syndrome Tests Genes GeneReviews	DEAFNESS WITH GOITER Goiter-deafness syndrome HYPOTHYROIDISM, CONGENITAL, DUE TO DYSHORMONOGENESIS, 2B Pendred's syndrome THYROID DYSHORMONOGENESIS 2B THYROID HORMONOGENESIS, GENETIC DEFECT IN, 2B
Select item 1641146	Long QT syndrome 1 Tests Gene GeneReviews
Select item 1684869	Epilepsy, idiopathic generalized, susceptibility to, 16 Tests Gene GeneReviews
Select item 761234	Autosomal recessive nonsyndromic hearing loss 4 Tests Genes GeneReviews	DEAFNESS, AUTOSOMAL RECESSIVE 4, WITH ENLARGED VESTIBULAR AQUEDUCT, DIGENIC Deafness, autosomal recessive 4 Deafness, autosomal recessive 4, with enlarged vestibular aqueduct Enlarged vestibular aqueduct, digenic FOXI1-Related Pendred Syndrome KCNJ10-Related Pendred Syndrome NEUROSENSORY NONSYNDROMIC RECESSIVE DEAFNESS 4 Nonsyndromic enlarged vestibular aqueduct (NSEVA)
Select item 460425	Seizures, benign familial neonatal, 1 Tests Gene GeneReviews	Benign Neonatal Epilepsy 1 KCNQ2-Related Benign Familial Neonatal Epilepsy
Select item 327586	Andersen Tawil syndrome Tests Gene GeneReviews	Andersen Syndrome Andersen cardiodysrhythmic periodic paralysis Long QT syndrome 7 Periodic paralysis, potassium-sensitive cardiodysrhythmic type Potassium-sensitive periodic paralysis, ventricular ectopy, and dysmorphic features
Select item 411243	EAST syndrome Tests Gene GeneReviews	Epilepsy, ataxia, sensorineural deafness and tubulopathy SEIZURES, SENSORINEURAL DEAFNESS, ATAXIA, IMPAIRED INTELLECTUAL DEVELOPMENT, AND ELECTROLYTE IMBALANCE SeSAME syndrome Seizures, Sensorineural Deafness, Ataxia, Mental Retardation, and Electrolyte Imbalance Syndrome Seizures, sensorineural deafness, ataxia, mental retardation and electrolyte imbalance
Select item 1646925	Jervell and Lange-Nielsen syndrome 1 Tests Gene GeneReviews	Cardioauditory syndrome of Jervell and Lange-Nielsen Deafness, congenital, and functional heart disease Prolonged QT interval in EKG and sudden death Surdo-cardiac syndrome
Select item 462293	Long QT syndrome 2 Tests Genes GeneReviews
Select item 373232	Atrial fibrillation, familial, 3 Tests Gene GeneReviews	KCNQ1-Related Familial Atrial Fibrillation
Select item 419173	Hyperinsulinemic hypoglycemia, familial, 2 Tests Gene GeneReviews	HYPERINSULINEMIC HYPOGLYCEMIA, PERSISTENT HYPERINSULINISM, NEONATAL KCNJ11-Related Hyperinsulinism
Select item 358092	Long QT syndrome 5 Tests Gene GeneReviews
Select item 413928	Brugada syndrome 8 Tests Gene GeneReviews
Select item 343428	Bartter disease type 2 Tests Gene GeneReviews	Bartter syndrome, type 2, antenatal HYPOKALEMIC ALKALOSIS WITH HYPERCALCIURIA 2, ANTENATAL Hyperprostaglandin E syndrome 2
Select item 462303	Long QT syndrome 6 Tests Gene GeneReviews
Select item 394108	Jervell and Lange-Nielsen syndrome 2 Tests Gene GeneReviews
Select item 462083	Long QT syndrome 13 Tests Gene GeneReviews

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