Clinical and research tests for 2,3-Difluoro-6-methoxybenzylamine - Genetic Testing Registry (GTR)

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Select all conditions on this page	Conditions	Synonyms
Select item 41523	Type 2 diabetes mellitus	DIABETES MELLITUS, TYPE 2, PROTECTION AGAINST Diabetes mellitus, noninsulin-dependent, late onset KCNJ11-Related Susceptibility to Noninsulin-Dependent Diabetes Mellitus Type II diabetes mellitus
Select item 48574	Schizophrenia
Select item 863175	Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 2	MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 2, SOMATIC
Select item 343561	Exudative vitreoretinopathy 1	Criswick-Schepens syndrome FEVR, AUTOSOMAL DOMINANT FZD4-Related Familial Exudative Vitreoretinopathy, Autosomal Dominant Familial exudative vitreoretinopathy, autosomal dominant
Select item 449382	Nonpapillary renal cell carcinoma
Select item 389187	Hepatocellular carcinoma	Hepatocellular cancer Hepatoma LIVER CELL CARCINOMA Primary carcinoma of liver
Select item 482302	Pregnancy loss, recurrent, susceptibility to, 2
Select item 482300	Pregnancy loss, recurrent, susceptibility to, 1	EMBRYONIC LOSS, RECURRENT FETAL LOSS, RECURRENT, SUSCEPTIBILITY TO MISCARRIAGE, RECURRENT STILLBIRTH, RECURRENT
Select item 209234	6-Pyruvoyl-tetrahydrobiopterin synthase deficiency	6-Pyruvoyltetrahydropterin Synthase Deficiency 6-pyruvoyl-tetrahydropterin synthase deficiency BH4-deficient hyperphenylalaninemia A HYPERPHENYLALANINEMIA, TETRAHYDROBIOPTERIN-DEFICIENT, DUE TO PTS DEFICIENCY Hyperphenylalanemia, BH4-deficient, A Hyperphenylalaninemia due to 6-pyruvoyl-tetrahydropterin synthase deficiency PTS Deficiency
Select item 815540	Ehlers-Danlos syndrome, spondylodysplastic type, 2	Ehlers-Danlos syndrome, progeroid type, 2
Select item 349087	Long QT syndrome 3	SCN5A-Related Romano Ward Syndrome
Select item 815800	Epidermolysis bullosa simplex 3, localized or generalized intermediate, with BP230 deficiency	Epidermolysis bullosa simplex due to BP230 deficiency Epidermolysis bullosa simplex, autosomal recessive 2
Select item 320428	Mycobacterium tuberculosis, susceptibility to
Select item 443951	Maple syrup urine disease type 1B	MSUD due to deficiency of e1-beta subunit of branched-chain alpha-keto acid dehydrogenase complex MSUD type 3 (formerly) MSUD type IB
Select item 370755	Febrile seizures, familial, 8	CONVULSIONS, FAMILIAL FEBRILE, 8 GABRG2-Related Generalized Epilepsy with Febrile Seizures Plus
Select item 941225	Deutetrabenazine response	Austedo response
Select item 898858	Optic atrophy 9
Select item 893186	Sofosbuvir response	Sovaldi response
Select item 68568	Spermatogenic failure 4	AZOOSPERMIA WITH MATURATION ARREST Arrest of spermatogenesis Azoospermia due to Perturbations of Meiosis PREGNANCY LOSS 4 Spermatogenesis arrest
Select item 482304	Pregnancy loss, recurrent, susceptibility to, 3

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