Clinical and research tests for Sedum chauveaudii - Genetic Testing Registry (GTR)

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Select all conditions on this page	Conditions	Synonyms
Select item 356466	Bilirubin, serum level of, quantitative trait locus 1
Select item 462105	Sodium serum level quantitative trait locus 1
Select item 481726	Transferrin serum level quantitative trait locus 2
Select item 69128	Elevated circulating creatine kinase concentration	CAV3-Related Isolated HyperCKemia Elevated serum creatine phosphokinase HYPERCKEMIA, IDIOPATHIC Isolated HyperCKemia
Select item 3925	Duchenne muscular dystrophy	Muscular dystrophy, pseudohypertrophic progressive, Duchenne type
Select item 443948	Malignant hyperthermia, susceptibility to, 1	Anesthesia related hyperthermia Fulminating hyperpyrexia Malignant hyperpyrexia Malignant hyperthermia suceptibility 1 Pharmacogenic myopathy RYR1-Related Malignant Hyperthermia Susceptibility
Select item 182959	Becker muscular dystrophy	Becker's muscular dystrophy Benign pseudohypertrophic muscular dystrophy Muscular dystrophy pseudohypertrophic progressive, Becker type
Select item 327063	IgE responsiveness, atopic	IMMUNOGLOBULIN E, BASIC LEVEL OF, IN SERUM
Select item 358309	Alkaline phosphatase, plasma level of, quantitative trait locus 1	ALKALINE PHOSPHATASE, ELEVATED SERUM HYPERPHOSPHATASEMIA, BENIGN FAMILIAL
Select item 358271	Inherited susceptibility to asthma	ASTHMA, BRONCHIAL ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO Asthma, susceptibility to
Select item 482271	Complement component 4b deficiency	Decreased circulating complement C4b concentration Decreased serum complement C4b
Select item 766407	Soluble interleukin-6 receptor, serum level of, quantitative trait locus	SOLUBLE IL6R, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS
Select item 393332	Uric acid concentration, serum, quantitative trait locus 4	GOUT SUSCEPTIBILITY 4
Select item 356333	Progressive familial intrahepatic cholestasis type 3	Low Gamma-GT Familial Intrahepatic Cholestasis MDR3 deficiency Progressive familial intrahepatic cholestasis with elevated serum gamma-glutamyltransferase
Select item 761697	Interleukin 6, serum level of, quantitative trait locus	IL6, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS
Select item 75677	Infantile hypophosphatasia
Select item 854011	Hemochromatosis type 1	HFE-Associated Hereditary Hemochromatosis
Select item 289648	Hypogonadotropic hypogonadism 2 with or without anosmia	HYPOGONADOTROPIC HYPOGONADISM 2 WITH OR WITHOUT ANOSMIA, SUSCEPTIBILITY TO HYPOGONADOTROPIC HYPOGONADISM 2 WITHOUT ANOSMIA HYPOGONADOTROPIC HYPOGONADISM 2 WITHOUT ANOSMIA, SUSCEPTIBILITY TO Kallmann syndrome 2
Select item 358391	Autosomal recessive limb-girdle muscular dystrophy type 2A	Calpainopathy Leyden-Moebius muscular dystrophy Limb-girdle muscular dystrophy type 2 Limb-girdle muscular dystrophy, type 2A Muscular dystrophy, limb-girdle, type 2A, Amish Muscular dystrophy, pelvofemoral
Select item 354935	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency	ADA deficiency ADA-SCID Adenosine Deaminase Deficiency Adenosine Deaminase-Deficient Severe Combined Immunodeficiency Disease (SCID) Adenosine deaminase deficient severe combined immunodeficiency SCID DUE TO ADA DEFICIENCY, EARLY-ONSET Severe combined immunodeficiency due to ADA deficiency Severe combined immunodeficiency due to adenosine deaminase deficiency

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