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

Warning: The NCBI web site requires JavaScript to function. more...

<< First< Prev

Page 1 of 5

Results: 1 to 20 of 81

Select all conditions on this page	Gene symbol	Associated conditionsHelp Conditions and phenotypes associated with each gene as reported by OMIM, GeneReviews and Gene
Select item 10058	ABCB6	Dyschromatosis universalis hereditaria 3 Familial pseudohyperkalemia Langereis blood group Microphthalmia, isolated, with coloboma 7
Select item 6833	ABCC8	Diabetes mellitus, permanent neonatal 3 Diabetes mellitus, transient neonatal, 2 Hyperinsulinemic hypoglycemia, familial, 1 Leucine-induced hypoglycemia Permanent neonatal diabetes mellitus Type 2 diabetes mellitus
Select item 38	ACAT1	Deficiency of acetyl-CoA acetyltransferase
Select item 208	AKT2	Hypoinsulinemic hypoglycemia and body hemihypertrophy Type 2 diabetes mellitus
Select item 144245	ALG10B	Long QT syndrome 2
Select item 779	CACNA1S	Congenital myopathy 18 Hypokalemic periodic paralysis, type 1 Malignant hyperthermia, susceptibility to, 5 Thyrotoxic periodic paralysis, susceptibility to, 1
Select item 1028	CDKN1C	Beckwith-Wiedemann syndrome IMAGe syndrome
Select item 1188	CLCNKB	Bartter disease type 3 Bartter disease type 4B
Select item 8452	CUL3	Neurodevelopmental disorder with or without autism or seizures Pseudohypoaldosteronism type 2E Pseudohypoaldosteronism, type 2
Select item 1586	CYP17A1	Deficiency of steroid 17-alpha-monooxygenase
Select item 5167	ENPP1	Arterial calcification, generalized, of infancy, 1 Hypophosphatemic rickets, autosomal recessive, 2 Hypopigmentation-punctate palmoplantar keratoderma syndrome Inherited obesity Type 2 diabetes mellitus
Select item 2299	FOXI1	Autosomal recessive nonsyndromic hearing loss 4 Pendred syndrome
Select item 2645	GCK	Hyperinsulinism due to glucokinase deficiency Maturity-onset diabetes of the young type 2 Permanent neonatal diabetes mellitus Permanent neonatal diabetes mellitus 1 Type 2 diabetes mellitus
Select item 2820	GPD2	Type 2 diabetes mellitus
Select item 105259599	H19-ICR	Beckwith-Wiedemann syndrome Silver-Russell syndrome 1 Wilms tumor 2
Select item 348980	HCN1	Developmental and epileptic encephalopathy, 24 Generalized epilepsy with febrile seizures plus, type 10
Select item 10021	HCN4	Brugada syndrome 8 Epilepsy, idiopathic generalized, susceptibility to, 18 Sick sinus syndrome 2, autosomal dominant
Select item 3159	HMGA1	Type 2 diabetes mellitus
Select item 6927	HNF1A	Diabetes mellitus type 1 Hepatic adenomas, familial Maturity-onset diabetes of the young type 3 Nonpapillary renal cell carcinoma Type 1 diabetes mellitus 20 Type 2 diabetes mellitus
Select item 6928	HNF1B	Nonpapillary renal cell carcinoma Renal cysts and diabetes syndrome Type 2 diabetes mellitus

<< First< Prev

Page 1 of 5

Next >Last >>

Results: 1 to 20 of 81

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.