Clinical and research tests for Tinus candolleana - Genetic Testing Registry (GTR)

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Select all conditions on this page	Conditions	Synonyms
Select item 320273	Sick sinus syndrome 2, autosomal dominant Tests Gene GeneReviews	ATRIAL FIBRILLATION WITH BRADYARRHYTHMIA SICK SINUS SYNDROME 2 SICK SINUS SYNDROME 2 WITH OR WITHOUT CARDIAC NONCOMPACTION AND/OR ASCENDING AORTA DILATION SINUS BRADYCARDIA SYNDROME, FAMILIAL, AUTOSOMAL DOMINANT SINUS NODE DISEASE, FAMILIAL, AUTOSOMAL DOMINANT
Select item 481421	Sick sinus syndrome 3, susceptibility to Tests Gene GeneReviews
Select item 325270	Sick sinus syndrome 1 Tests Gene GeneReviews	SICK SINUS SYNDROME, CONGENITAL SINUS BRADYCARDIA SYNDROME, FAMILIAL SINUS NODE DISEASE, FAMILIAL, AUTOSOMAL RECESSIVE SINUS RHYTHM, CONGENITAL ABSENCE OF Sick sinus syndrome 1, autosomal recessive
Select item 400532	H syndrome Tests Gene GeneReviews	Asrar Facharzt Haque syndrome Faisalabad histiocytosis HISTIOCYTOSIS AND LYMPHADENOPATHY WITH OR WITHOUT CUTANEOUS, CARDIAC, AND/OR ENDOCRINE FEATURES, JOINT CONTRACTURES, AND/OR DEAFNESS HYPERPIGMENTATION, CUTANEOUS, WITH HYPERTRICHOSIS, HEPATOSPLENOMEGALY, HEART ANOMALIES, AND HYPOGONADISM WITH OR WITHOUT HEARING LOSS Histiocytosis with joint contractures and sensorineural deafness Histiocytosis-lymphadenopathy plus syndrome Hyperpigmentation, Cutaneous, with Hypertrichosis, Hepatosplenomegaly, Heart Anomalies, Hearing Loss, and Hypogonadism PIGMENTED HYPERTRICHOSIS WITH INSULIN-DEPENDENT DIABETES MELLITUS Pigmented hypertrichosis and insulin-dependent diabetes mellitus ROSAI-DORFMAN DISEASE, FAMILIAL SINUS HISTIOCYTOSIS AND MASSIVE LYMPHADENOPATHY
Select item 120524	Holt-Oram syndrome Tests Gene GeneReviews	Atrio digital syndrome Cardiac-limb syndrome HOS 1 Heart-hand syndrome, type 1 TBX5-Related Holt-Oram Syndrome Ventriculo-radial syndrome
Select item 1640616	Van der Woude syndrome 1 Tests Gene GeneReviews	Cleft lip and/or palate with mucous cysts of lower lip
Select item 3486	Cleidocranial dysostosis Tests Gene GeneReviews	CLEIDOCRANIAL DYSPLASIA 1 Cleidocranial Dysplasia Marie-Sainton disease
Select item 1646402	Brugada syndrome 1 Tests Gene GeneReviews	Right bundle branch block, ST segment elevation, and sudden death syndrome SCN5A-Related Brugada Syndrome
Select item 395633	Brugada syndrome 3 Tests Gene GeneReviews
Select item 1794285	Central hypoventilation syndrome, congenital, 1, with or without Hirschsprung disease Tests Gene GeneReviews	AUTONOMIC CONTROL, CONGENITAL FAILURE OF CENTRAL HYPOVENTILATION SYNDROME, CONGENITAL, 1 ONDINE CURSE, CONGENITAL
Select item 413928	Brugada syndrome 8 Tests Gene GeneReviews
Select item 395632	Brugada syndrome 4 Tests Gene GeneReviews
Select item 222975	Brugada syndrome Tests Genes GeneReviews	Sudden Unexplained Death Syndrome Sudden Unexplained Nocturnal Death Syndrome (SUNDS) Sudden unexpected nocturnal death syndrome Sudden unexplained nocturnal death syndrome
Select item 413472	Brugada syndrome 7 Tests Gene GeneReviews
Select item 411607	Brugada syndrome 5 Tests Gene GeneReviews
Select item 220902	Congenital central hypoventilation Tests Genes GeneReviews	Congenital Central Hypoventilation Syndrome Congenital failure of autonomic control Idiopathic congenital central alveolar hypoventilation Primary alveolar hypoventilation
Select item 20749	Sick sinus syndrome Tests Genes GeneReviews
Select item 413473	Brugada syndrome 6 Tests Gene GeneReviews
Select item 382031	Brugada syndrome 2 Tests Gene GeneReviews
Select item 2039	Cardiac arrhythmia Tests Genes GeneReviews	Cardiac rhythm disease

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