Disease Organ Panels
Disease Organ Panels
Disease Organ Panels
Anemia
CBC with indices, reticulocyte count and microscopic examination
Microcytic: Iron, ESR
Normocytic: ESR, hemolysis profile
Macrocytic: B12, folate, TSH
Coagulation Screening
Prothrombin time
Thrombin time
Partial thromboplastin time
Platelet count
Platelet function test
Hemolysis
CBC
Bilirubin
Haptoglobin
Free hemoglobin (plasma and urine)
Lactate dehydrogenase (LD)
Direct Antiglobulin Test
Reticulocyte count
Arthritis
ESR (sedimentation rate)
Uric acid
ANA
C-reactive protein
Rheumatoid factor
Cyclic citrullinated peptide antibody
Bone/Joint
Albumin
Calcium
Phosphorus
Osteocalcin
Protein, total
Uric acid
Alkaline phosphatase
25-OH Vitamin D
Cardiac Injury
Collagen Disease/SLE
ESR
C-reactive protein
C3
C4
ANCA (antibody neutrophil cytoplasmic antibody)
ANA
Anti-DNA
Coma
Basic Metabolic Panel
Toxicology screen
Salicylate
Ammonia
Anion gap
Arterial blood gas profile
Alcohol
Lactic acid
Calcium (total and ionized)
Serum osmolality
Electrolyte/Fluid Management
Basic Metabolic Panel
Plasma and urine osmolality
Creatinine clearance
Free water clearance
Anion gap
General Health
CBC
Comprehensive Metabolic Panel
Lipid Panel
Uric acid
TSH
Hypertension
Basic Metabolic Panel
Urinary free cortisol
Renin
Thyroid Screening
Urinary metanephrines
Urinalysis
Iron/Hemochromatosis
Serum iron
TIBC (total iron-binding capacity)
% Saturation
Ferritin
Alanine Amino Transferase (ALT)
Hepatic Function
Albumin
Prothrombin time
Bilirubin (total and direct)
GGT
Protein, total
Alanine Amino Transferase (ALT)
Aspartate Amino Transferase (AST)
Alkaline phosphatase
Newborn Screening
Argininosuccinic acidemia (ASA)
Beta-Ketothiolase deficiency (ßKT)
Biotinidase deficiency (BIOT)
Carnitine uptake defect (CUD)
Citrullinemia (CIT)
Congenital adrenal hyperplasia (CAH)
Congenital hypothyroidism (CH)
Cystic fibrosis (CF)
Galactosemia (GALT)
Glutaric acidemia type I (GA I)
Hemoglobin Sickle/Beta-thalassemia (HbS/ßTh)
Hemoglobin Sickle/C disease (Hb S/C)
Homocystinuria (HCY)
Isovaleric acidemia (IVA)
Long chain hydroxyacyl-CoA dehydrogenase
deficiency (LCHAD)
Maple syrup urine disease (MSUD)
Medium-chain acyl-CoA dehydrogenase
deficiency (MCAD)
Methylmalonic acidemia (mutase deficiency) (MUT)
Methylmalonic acidemia (Cbl A,B)
Multiple carboxylase deficiency (MCD)
Pancreatic
Amylase
Calcium (total and ionized)
Triglycerides
Lipase
Glucose
Parathyroid
Albumin
Alkaline phosphatase
Magnesium
Creatinine
PTH (whole molecule, amino terminal)
Protein, total
Calcium (total and ionized)
Phosphorus
Urinary calcium
Prenatal Screening
CBC
BUN
Uric Acid
ABO and Rh typing
Urinalysis
Toxoplasmosis Ab
CMV Ab
Hepatitis B surface Ag
HIV antibody
Cervical Pap smear
Cervical culture/amplification for GC,
Chlamydia, group B Streptococci
Glucose
Creatinine
Free T4
Erythrocyte Antibody screen
Urine culture
Rubella titer
Syphilis serology (RPR)
Herpes simplex I & II Ab
Renal
Basic Metabolic Panel
Magnesium
Albumin
24-hr urine protein
Creatinine clearance
Phosphorus
Protein, total
24-hr creatinine
CBC