Clinical and research tests for 1,1,1-Trichlorobutane - Genetic Testing Registry (GTR)

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Select all conditions on this page	Conditions	Synonyms
Select item 412713	Neuroblastoma, susceptibility to, 1	Neuroblastoma 1
Select item 463619	IgA nephropathy, susceptibility to, 1	IGAN1
Select item 382914	Breast-ovarian cancer, familial, susceptibility to, 1	BRCA1 Hereditary Breast and Ovarian Cancer Breast cancer, familial 1 OVARIAN CANCER, SUSCEPTIBILITY TO
Select item 41522	Diabetes mellitus type 1	Type I diabetes mellitus
Select item 412743	Hemolytic uremic syndrome, atypical, susceptibility to, 1	AHUS, SUSCEPTIBILITY TO, 1 Atypical hemolytic-uremic syndrome 1
Select item 325315	Myocardial infarction, susceptibility to, 1	Myocardial infarction 1
Select item 409531	Gaucher disease type I	Acid beta-glucosidase deficiency GBA DEFICIENCY GD 1 GD I Gaucher disease type 1 Gaucher disease, noncerebral juvenile Gaucher's disease, type 1 Glucocerebrosidase deficiency
Select item 18013	Neurofibromatosis, type 1	NEUROFIBROMATOSIS, TYPE I NEUROFIBROMATOSIS, TYPE I, SOMATIC Peripheral type neurofibromatosis Recklinghausen's disease Von Recklinghausen disease
Select item 45811	Familial Mediterranean fever	Benign paroxysmal peritonitis Familial Mediterranean Fever Type 1 Familial Mediterranean Fever Type 2 POLYSEROSITIS, FAMILIAL PAROXYSMAL POLYSEROSITIS, RECURRENT Periodic disease Periodic peritonitis
Select item 422452	Bardet-Biedl syndrome 1
Select item 162917	Simpson-Golabi-Behmel syndrome type 1	Bulldog syndrome Dysplasia gigantism syndrome, X-linked GPC3-Related Simpson-Golabi-Behmel Syndrome Type 1 Golabi-Rosen syndrome Simpson dysmorphia syndrome
Select item 356466	Bilirubin, serum level of, quantitative trait locus 1
Select item 155703	Spinocerebellar ataxia type 1	CEREBELLOPARENCHYMAL DISORDER I Cerebelloparenchymal disorder 1 OLIVOPONTOCEREBELLAR ATROPHY I OLIVOPONTOCEREBELLAR ATROPHY IV Olivopontocerebellar atrophy 1 Olivopontocerebellar atrophy 4 SPINOCEREBELLAR ATROPHY I Spinocerebellar atrophy 1
Select item 462105	Sodium serum level quantitative trait locus 1
Select item 9957	Multiple endocrine neoplasia, type 1	Endocrine adenomatosis multiple MEA I MEN 1 MEN I Wermer syndrome
Select item 124337	Glutaric aciduria, type 1	GA I Glutaric acidemia type 1 Glutaric acidemia type I Glutaricacidemia Type 1 Glutaricaciduria, type I Glutaryl-CoA dehydrogenase deficiency
Select item 394222	SKIN/HAIR/EYE PIGMENTATION 3, LIGHT/DARK SKIN	EYE COLOR 1 EYE COLOR, GREEN/BLUE SKIN/HAIR/EYE PIGMENTATION 3, BLUE/GREEN EYE COLOR SKIN/HAIR/EYE PIGMENTATION 3, FRECKLING Skin/hair/eye pigmentation, variation in, 3
Select item 423615	Lynch syndrome 1	COLON CANCER, FAMILIAL NONPOLYPOSIS, TYPE 1 Colorectal cancer, hereditary, nonpolyposis, type 1 Hereditary non-polyposis colorectal cancer, type 1 Lynch syndrome I MSH2-Related Hereditary Non-Polyposis Colon Cancer MSH2-Related Lynch Syndrome
Select item 886881	Steinert myotonic dystrophy syndrome	Dystrophia myotonica type 1 Myotonic dystrophy type 1 Steinert disease Steinert myotonic dystrophy Steinert's disease
Select item 332156	Susceptibility to HIV infection	HIV-1, SUSCEPTIBILITY TO HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, RESISTANCE TO Human immunodeficiency virus type 1, susceptibility to

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