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Find COVID-19 Information and Resources
Information from TN Dept of Health about the Ongoing Novel Coronavirus Outbreak

Laboratory Directory of Services

Disease, Suspected Agent or Requested Test
Alphabetical Directory

Click on the letters below to browse the test menu

Fecal coliform

Foodborne illness outbreak - contact CEDEP for guidance

Francisella tularensis

Fungus culture (Mycology)

LaCrosse encephalitis virus (California Group)

Legionella pneumophila, culture

Legionella, environmental sample

Legionnaires diseases—Legionella

Listeria species

Organic Chemistry—Environmental Laboratories

Orthopox

Ova and parasites—Parasites, Intestinal

Q fever (Coxiella burnetii)

Quantiferon Gold - Tuberculosis

Total coliform

TP-PA (Treponema pallidum Particle Agglutination)—Syphilis Serology

Tuberculosis (TB)—Mycobacterium tuberculosis

Tularemia—Francisella tularensis


Undulant fever—Brucella species

Water bacteriology

Water chemistry

West Nile Virus Encephalitis Serology -Human

West Nile Virus-Birds and Mosquitos

2 Methyl 3 Hydroxy Butyric Aciduria (2M3HBA)

2,4 Dienyl CoA Reductase Deficiency (DE RED)

2-Methylbutyryl-CoA Dehydrogenase Deficiency (2MBCD)

3 Hydroxy 3 Methylglutaric Aciduria (HMG)

3 Methyl Crotonyl CoA Carboxylase Deficiency (3 MCC)

3 Methylglutaconyl CoA Hydratase Deficiency (3MGA)

β Ketothiolase Deficiency  (SKAT)

Argininemia (ARG)

Argininosuccinic Aciduria (ASA)


Biotinidase Deficiency

Carbamoyl Phosphate Synthetase I Deficiency (CPS I)

Carnitine Acylcarnitine Translocase Deficiency (CACTD)

Carnitine Palmitoyltransferase Type I Deficiency (CPT I)

Carnitine Palmitoyltransferase Type II Deficiency (CPTII)

Carnitine Uptake Defect (CUD)

Citrullinemia Type I (CIT)

Citrullinemia Type II (CIT II)

Congenital Adrendal Hyperplasia I (CAH)

Congenital Hypothyroidism (CH)

Cystic Fibrosis (CF) 

Fabry Disease

Galactokinase Deficiency


Galactose Epimerase Deficiency

Galactosemia 

Gaucher Disease

Glutaric Acidemia Type I (GA-1)

Glutaric Acidemia Type II (GA -2)

Homocystinuria (HCY)

Hypermethioninemia (MET)

Hyperornithinemia (HHH)

Hyperphenylalaninemia (H-PHE)

Isobutyrylglycinuria 

Isovaleric Acidemia

Krabbe Disease

Long Chain L-3 Hydroxylacyl-CoA Dehydrogenase Deficiency

Malonic Acidemia

Maple Syrup Urine Disease (MSUD)


Medium Chain AcylCoA Dehydrogenase Deficiency (MCAD)

Medium/Short chain L-3 hydroxyacyl CoA Dehydrogenase Deficiency (M/SCHAD)

Methylmalonic Acidemia (MMA)

Mucopolysaccharidosis Type I (MPS I)

Multiple CoA Carboxylase Deficiency (MCD)

Nonketotic Hyperglycinemia (NKH)

Ornithine Transcarbamylase Deficiency (OTC)

Phenylketonuria   (PKU)

Pompe Disease

Propionic Acidemia (PROP)

SC Disease

Severe Combine immunodeficiency (SCID)

Short Chain AcylCoA Dehydrogenase Deficiency (SCAD)


Sickle Beta Thalassemia

Sickle Cell Anemia

Spinal Muscular Atrophy Type I (SMA)


Spinal Muscular Atrophy Type II (SMA)

Spinal Muscular Atrophy Type III (SMA)

Spinal Muscular Atrophy Type VI (SMA)

Trifunctional Protein Deficiency (TFP)

Tyrosinemia Type 1

Tyrosinemia Type 2


Tyrosinemia Type 3

Very Long Chain AcylCoA Dehydrogenase Deficiency (VLCAD)

X-linked Adrenoleukodystrophy


 Requisitions: