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Results: 1 to 20 of 312

Make selection to find tests for any of the checked conditions.[x]
ConditionsSynonyms
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
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
Gaucher disease type III
  • GD 3
  • GD III
  • Gaucher Disease Type 3 (Subacute/Chronic)
  • Gaucher Disease, Type 3
  • Gaucher disease, chronic neuronopathic type
  • Gaucher disease, juvenile and adult, cerebral
  • Gaucher disease, subacute neuronopathic type
  • Subacute neuronopathic Gaucher's disease
Meckel syndrome, type 1
  • MECKEL-GRUBER SYNDROME, TYPE 1
  • MKS1-Related Meckel Syndrome
3-methylcrotonyl-CoA carboxylase 1 deficiency
  • 3 Alpha methylcrotonylglycinuria 1
  • MCC 1 deficiency
  • MCCC1-Related 3-Methylcrotonyl-CoA Carboxylase Deficiency
  • MCCD TYPE 1
  • METHYLCROTONYLGLYCINURIA TYPE I
Hereditary spastic paraplegia 3A
  • FAMILIAL SPASTIC PARAPLEGIA, AUTOSOMAL DOMINANT, 1
  • SPASTIC PARAPLEGIA 3, AUTOSOMAL DOMINANT
  • SPG3
  • Spastic Paraplegia 3A
  • Spastic paraplegia 3
  • Spastic paraplegia 3A, autosomal dominant
  • Strumpell disease
Gaucher disease
  • Acute cerebral Gaucher disease
  • Cerebroside lipidosis syndrome
  • Gaucher splenomegaly
  • Glucocerebrosidosis
  • Glucosyl cerebroside lipidosis
  • Glucosylceramidase deficiency
  • Kerasin lipoidosis
  • Kerasin thesaurismosis
  • Sphingolipidosis 1
3-methylglutaconic aciduria type 1
  • 3 alpha methylglutaconic aciduria type I
  • 3 methylglutaconic aciduria type I
  • 3 methylglutaconyl CoA hydratase deficiency
  • 3MG CoA hydratase deficiency
  • MGA type I
von Willebrand disease type 1
  • VON WILLEBRAND DISEASE, TYPE I
  • VWD, TYPE 1
Autosomal dominant centronuclear myopathy
  • MYOTUBULAR MYOPATHY, AUTOSOMAL DOMINANT
  • Myopathy, centronuclear, 1
  • Myopathy, centronuclear, 3
Porokeratosis 3, disseminated superficial actinic type
  • POROKERATOSIS 3, MIBELLI TYPE
  • POROKERATOSIS 3, MULTIPLE TYPES
  • POROKERATOSIS, DISSEMINATED SUPERFICIAL ACTINIC, 1
Bardet-Biedl syndrome 1
Achromatopsia 3
  • ACHM1 (formerly)
  • Achromatopsia with myopia
  • Pingelapese blindness
  • RMCH1 (formerly)
  • ROD MONOCHROMACY 1
  • ROD MONOCHROMATISM 1
  • Rod monochromacy 1 (formerly)
  • Rod monochromatism 1 (formerly)
  • Total colorblindness with myopia
Exudative vitreoretinopathy 1
  • Criswick-Schepens syndrome
  • FEVR, AUTOSOMAL DOMINANT
  • FZD4-Related Familial Exudative Vitreoretinopathy, Autosomal Dominant
  • Familial exudative vitreoretinopathy, autosomal dominant
Axenfeld-Rieger syndrome type 3
  • AXENFELD-RIEGER ANOMALY WITH CARDIAC DEFECTS AND/OR SENSORINEURAL HEARING LOSS
  • Anterior chamber cleavage syndrome
  • Axenfeld-rieger anomaly with or without cardiac defects and/or sensorineural hearing loss
  • Rieger syndrome type 3
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
Susceptibility to HIV infection
  • HIV-1, SUSCEPTIBILITY TO
  • HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, RESISTANCE TO
  • Human immunodeficiency virus type 1, susceptibility to
Polyglandular autoimmune syndrome, type 1
  • APS 1
  • APS I
  • AUTOIMMUNE POLYENDOCRINE SYNDROME, TYPE I, WITH OR WITHOUT REVERSIBLE METAPHYSEAL DYSPLASIA
  • Autoimmune Polyendocrinopathy Syndrome Type 1
  • Autoimmune polyendocrine syndrome type 1
  • Autoimmune polyendocrinopathy syndrome, type I
  • Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED)
  • Hypoadrenocorticism with hypoparathyroidism and superficial moniliasis
  • PGA 1
  • PGA I
  • Whitaker syndrome
Alzheimer disease 3
  • ALZHEIMER DISEASE, FAMILIAL, 3
  • Alzheimer disease early onset type 3
Nephronophthisis 1
  • Nephronophthisis familial juvenile

Results: 1 to 20 of 312

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