Clinical and research tests for IGKV1D-8 - Genetic Testing Registry (GTR)

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Results: 1 to 20 of 543

Select all conditions on this page	Conditions	Synonyms
Select item 414549	Epilepsy, idiopathic generalized, susceptibility to, 8 Tests Gene GeneReviews	Epilepsy, idiopathic generalized 8
Select item 98158	Trisomy 8 Tests Genes GeneReviews	Chromosome 8 duplication Chromosome 8, trisomy
Select item 463554	Melanoma, cutaneous malignant, susceptibility to, 8 Tests Gene GeneReviews	Cutaneous malignant melanoma 8 MELANOMA AND RENAL CELL CARCINOMA, SUSCEPTIBILITY TO
Select item 5501	Hereditary factor VIII deficiency disease Tests Gene GeneReviews	Factor 8 deficiency, congenital Factor VIII deficiency, congenital HEM A Hemophilia A Hemophilia A, congenital Hemophilia, classic
Select item 339628	Autosomal dominant Parkinson disease 8 Tests Gene GeneReviews	LRRK2-Related Parkinson Disease Parkinson disease 8 Parkinson disease 8, susceptibility to
Select item 1646997	Encephalopathy, acute, infection-induced (herpes-specific), susceptibility to, 8 Tests Gene GeneReviews	HERPES SIMPLEX ENCEPHALITIS, SUSCEPTIBILITY TO, 6
Select item 854172	Glycogen storage disease IXa1 Tests Gene GeneReviews	GSD VIII Glycogen storage disease 8 Glycogenosis type 8 Hepatic phosphorylase kinase deficiency LIVER GLYCOGENOSIS, X-LINKED, TYPE I PHKA2-Related Phosphorylase Kinase Deficiency Phosphorylase kinase deficiency of liver X-linked Liver Glycogenosis Type 1 X-linked Liver Glycogenosis Type 2
Select item 315656	Rapp-Hodgkin ectodermal dysplasia syndrome Tests Gene GeneReviews	Ectodermal dysplasia, anhidrotic, with cleft lip/palate Isolated Cleft Lip/Cleft Palate (Orofacial Cleft 8) Rapp-Hodgkin syndrome
Select item 412966	Lynch syndrome 8 Tests Gene GeneReviews	Colorectal cancer, hereditary nonpolyposis, type 8
Select item 342845	Maturity-onset diabetes of the young type 8 Tests Gene GeneReviews	Diabetes and pancreatic exocrine dysfunction Diabetes mellitus MODY type 8 Diabetes-pancreatic exocrine dysfunction syndrome Maturity-Onset Diabetes of the Young Type 8, with Exocrine Dysfunction
Select item 338613	Infantile onset spinocerebellar ataxia Tests Gene GeneReviews	Mitochondrial DNA depletion syndrome 7 (hepatocerebral type) OPHTHALMOPLEGIA, HYPOTONIA, ATAXIA, HYPOACUSIS, AND ATHETOSIS Ophthalmoplegia, hypotonia, ataxia, hypacusis, and athetosis SCA8 (formerly) Spinocerebellar ataxia 8 (formerly) Spinocerebellar ataxia infantile with sensory neuropathy
Select item 419136	Partial duplication of chromosome 8 Tests Genes GeneReviews
Select item 1825961	Partial deletion of chromosome 8 Tests Genes GeneReviews
Select item 1826035	Partial duplication of the long arm of chromosome 8 Tests Genes GeneReviews
Select item 815563	Noonan syndrome 8 Tests Gene GeneReviews
Select item 370192	Coronary heart disease, susceptibility to, 8 Tests Genes GeneReviews	CHDS8 Coronary heart disease 8
Select item 78750	Sarcotubular myopathy Tests Gene GeneReviews	Autosomal recessive limb-girdle muscular dystrophy type 2H Hutterite type of muscular dystrophy Limb-Girdle Muscular Dystrophy Type 2H MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 8 Muscular dystrophy Hutterite type
Select item 324806	Hypertrophic cardiomyopathy 8 Tests Gene GeneReviews	CARDIOMYOPATHY, HYPERTROPHIC, MID-LEFT VENTRICULAR CHAMBER TYPE, 1 Familial hypertrophic cardiomyopathy 8 MYL3-Related Familial Hypertrophic Cardiomyopathy
Select item 325237	Amyotrophic lateral sclerosis type 8 Tests Gene GeneReviews	VAPB-Related Amyotrophic Lateral Sclerosis
Select item 462552	Leber congenital amaurosis 8 Tests Gene GeneReviews	CRB1-Related Leber Congenital Amaurosis

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