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Results: 1 to 20 of 32

Make selection to find tests for any of the checked conditions.[x]
ConditionsSynonyms
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
Metaphyseal chondrodysplasia, Schmid type
  • SPONDYLOMETAPHYSEAL DYSPLASIA, JAPANESE TYPE
Combined deficiency of sialidase AND beta galactosidase
  • CATHEPSIN A DEFICIENCY
  • Cathepsin A deficiency of
  • Galactosialidosis
  • Goldberg syndrome
  • Lysosomal protective protein deficiency of
  • Neuraminidase deficiency with beta-galactosidase deficiency
  • Neuraminidase/beta-galactosidase expression
  • Protective protein/Cathepsin A deficiency
Thyrotoxic periodic paralysis, susceptibility to, 1
Ocular albinism, type I
  • Nettleship-Falls type ocular albinism
  • Ocular Albinism, X-Linked
  • Ocular albinism type 1
  • Ocular albinism, type I, Nettleship-Falls type
  • X-linked recessive ocular albinism
Gelatinous droplike corneal dystrophy
  • Amyloid corneal dystrophy, Japanese type
  • Corneal Dystrophy, Gelatinous Drop-Like
  • Corneal dystrophy, Lattice type 3
Symmetrical dyschromatosis of extremities
  • Dyschromatosis symmetrica hereditaria
  • Dyschromatosis symmetrica hereditaria 1
  • Familial reticulate acropigmentation of Dohi
  • Reticulate acropigmentation of Dohi
  • Symmetric dyschromatosis of the extremities
Moyamoya disease 5
Proteasome-associated autoinflammatory syndrome 1
  • AUTOINFLAMMATION, LIPODYSTROPHY, AND DERMATOSIS SYNDROME
  • CHRONIC ATYPICAL NEUTROPHILIC DERMATOSIS WITH LIPODYSTROPHY AND ELEVATED TEMPERATURE SYNDROME
  • JMP SYNDROME
  • JOINT CONTRACTURES, MUSCULAR ATROPHY, MICROCYTIC ANEMIA, AND PANNICULITIS-INDUCED LIPODYSTROPHY
  • NAKAJO-NISHIMURA SYNDROME
  • Nakajo syndrome
  • Nodular erythema digital changes
Lipoprotein glomerulopathy
Butyrylcholinesterase deficiency, fluoride-resistant, Japanese type
Japanese encephalitis virus disease
  • Japanese encephalitis
Spondylometaphyseal dysplasia, Schmidt type
  • Japanese type spondylometaphyseal dysplasia
  • Schmid metaphyseal dysostosis
  • Spondylometaphyseal dysplasia Algerian type
  • Spondylometaphyseal dysplasia with severe genu valgum
Dyschromatosis universalis hereditaria 1
Palmoplantar keratoderma, Nagashima type
Acatalasemia, japanese type
APRT deficiency, Japanese type
Moyamoya disease
  • Moyamoya syndrome
Satoyoshi syndrome
  • Komuragaeri Disease
  • Muscle spasms, intermittent with alopecia, diarrhea and skeletal abnormalities
Metaphyseal dysplasia, Braun-Tinschert type

Results: 1 to 20 of 32

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