Clinical and research tests for K Dragnev - Genetic Testing Registry (GTR)

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Results: 1 to 20 of 38

Select all conditions on this page	Conditions	Synonyms
Select item 900808	Migraine, with or without aura, susceptibility to, 13 Tests Gene GeneReviews	MIGRAINE WITH AURA, SUSCEPTIBILITY TO, 13 Migraine, with or without aura 13
Select item 1253	Abetalipoproteinaemia Tests Gene GeneReviews	Abetalipoproteinemia Abetalipoproteinemia neuropathy Apolipoprotein B deficiency Bassen Kornzweig syndrome Betalipoprotein deficiency disease Congenital betalipoprotein deficiency syndrome Low-density beta lipoprotein deficiency MTP DEFICIENCY Microsomal triglyceride transfer protein deficiency disease Microsomal-triglyceride transfer protein deficiency
Select item 815528	Pulmonary hypertension, primary, 4 Tests Gene GeneReviews
Select item 356333	Progressive familial intrahepatic cholestasis type 3 Tests Gene GeneReviews	Low Gamma-GT Familial Intrahepatic Cholestasis MDR3 deficiency Progressive familial intrahepatic cholestasis with elevated serum gamma-glutamyltransferase
Select item 393583	Birk-Barel syndrome Tests Gene GeneReviews	Birk Barel mental retardation dysmorphism syndrome Mental retardation with hypotonia and facial dysmorphism
Select item 450439	Cetuximab response Tests Genes GeneReviews	Erbitux response
Select item 1710473	LIPOPROTEIN(a) QUANTITATIVE TRAIT LOCUS Tests Gene GeneReviews
Select item 324817	Glaucoma 1, open angle, K Tests Genes GeneReviews	GLAUCOMA, PRIMARY OPEN ANGLE, JUVENILE-ONSET, 3 GLC1K
Select item 766918	Peroxisome biogenesis disorder 13A (Zellweger) Tests Gene GeneReviews	Peroxisome biogenesis disorder 13A
Select item 303176	Autosomal dominant chondrodysplasia punctata Tests Genes GeneReviews	CHONDRODYSPLASIA PUNCTATA DUE TO VITAMIN K DEFICIENCY
Select item 1781366	Hypercholanemia, familial 1 Tests Gene GeneReviews	BAAT-Related Familial Hypercholanemia
Select item 383840	Congenital bile acid synthesis defect 2 Tests Gene GeneReviews	Cholestasis with delta(4)-3-oxosteroid 5-beta-reductase deficiency
Select item 348876	Overhydrated hereditary stomatocytosis Tests Gene GeneReviews	Potassium sodium disorder of erythrocyte Stomatocytosis I
Select item 376381	Vitamin K-dependent clotting factors, combined deficiency of, type 1 Tests Gene GeneReviews	FACTORS II, VII, IX, AND X, COMBINED DEFICIENCY OF FAMILIAL MULTIPLE COAGULATION FACTOR DEFICIENCY III FMFD III GLUTAMIC ACID, DEFICIENT GAMMA-CARBOXYLATION OF MULTIPLE COAGULATION FACTOR DEFICIENCY III VITAMIN K-DEPENDENT COAGULATION DEFECT
Select item 208651	Chylomicron retention disease Tests Gene GeneReviews	Hypobetalipoproteinemia with accumulation of apolipoprotein b-like protein in intestinal cells Lipid transport defect of intestine
Select item 75668	Progressive familial intrahepatic cholestasis Tests Genes GeneReviews	Progressive family intrahepatic cholestasis Progressive intrahepatic cholestasis
Select item 324588	Familial pseudohyperkalemia Tests Gene GeneReviews	CRYOHYDROCYTOSIS, MILD PSEUDOHYPERKALEMIA EAST LONDON PSEUDOHYPERKALEMIA LILLE Pseudohyperkalemia Chiswick Pseudohyperkalemia Falkirk Pseudohyperkalemia, familial, 2, due to red cell leak
Select item 334505	Vitamin K-dependent clotting factors, combined deficiency of, type 2 Tests Gene GeneReviews
Select item 1780531	Hypercholanemia, familial, 2 Tests Gene GeneReviews	NTCP deficiency
Select item 1780260	Bile acid conjugation defect 1 Tests Gene GeneReviews

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