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LabMed
Abnormal Liver Function Tests: Elevated Serum Bilirubin and/or Predominant Elevations in ALP, 5'-NT, and/or Gamma Glutamyltransferase (GGT)
Abnormal Liver Function Tests: Elevations in ALT and AST, Which Predominate Over Elevations of Alkaline Phosphatase (ALP), 5'-NT, and/or Gamma Glutamyltransferase (GGT)
Abnormal Platelet Aggregation Studies
Abnormal Test Result in the Lipid Profile
Acute Coronary Syndrome (ACS)
Acute Myeloid Leukemias (AMLs)
Acute Pharyngitis
Acute Rheumatic Fever (ARF)
Acute Tubular Necrosis (ATN)
Addison's Disease (AD)
Adenosine Deaminase (ADA) Deficiency
Adrenocortical Carcinoma (ACC)
Alcoholic Liver Disease (ALD)
Alkaptonuria
Allergic Bronchopulmonary Aspergillosis (ABPA)
Allergy
Alpha-Thalassemias
Alport Syndrome
Alport Syndrome
Altered Urinary pH
Amyotrophic Lateral Sclerosis (ALS)
An Elevated Value for Human Chorionic Gonadotropin (hCG)
An Elevated Value of Troponin I, Troponin T, CK-MB, and/or Myoglobin
Anaplastic Large Cell Lymphoma (ALCL)
Androgen Insensitivity Syndrome (AIS)
Anemia Associated with Hemoglobin C
Anemia Associated with Hemoglobin D
Anemia Associated with Hemoglobin E
Anemia Associated with Hemoglobin G-Philadelphia
Anemia Associated with Hemoglobin Köln
Anemia Associated with Hemoglobin Lepore
Anemia Associated with Hemoglobin O-Arab
Anemia Associated with Hemoglobin S-Alpha Thalassemia
Anemia Associated with Hemoglobin S-Beta Thalassemia
Anemia Associated with Hemoglobin S-C
Anemia Associated with Hemoglobin S-D Los Angeles
Anemia Associated with Hemoglobin S-Hereditary Persistence of Fetal Hemoglobin
Anemia Associated with Hemoglobin S-O Arab
Anemia Associated with Lead Poisoning
Anemia of Chronic Disease (ACD)
Angina Pectoris
Angioimmunoblastic T Cell Lymphoma (AITL)
Anterior Pituitary, Growth Hormone (GH) Deficiency
Anterior Pituitary, Prolactin Deficiency
Anti-Neutrophils Cytoplasmic Antibodies (ANCA) Associated Vasculitis
Antiphospholipid Antibody Syndrome
Antiplasmin Deficiency
Antithrombin Deficiency
Atrophic Thyroiditis
Autoimmune Hemolytic Anemias
Autosomal Agammaglobulinemia
BUN and/or Creatinine Increased: Intrarenal Cause
BUN and/or Creatinine Increased: Postrenal Cause
BUN and/or Creatinine Increased: Prerenal Cause
Bartter Syndrome
Bernard-Soulier Disease (BSS)
Beta Thalassemias
Bilateral Hyperplasia of the Adrenal Gland
Bilirubinuria
Bleeding Associated with Warfarin Therapy
Bone Marrow Hypoplasia from Bone Marrow Replacement
Bone Marrow Hypoplasia from Bone Marrow Suppression
Burkitt Lymphoma Symptoms and Diagnosis
CDS:LABMED:Template1
CDS:LABMED:Template:Quick Glance
Canavan Disease
Carbamoylphosphate Synthetase Deficiency (CPS1)
Carcinoid
Casts in the Urine
Central Hypothyroidism – Hypopituitary, Hypothalamic, and Thyroid Stimulating Hormone (TSH) Deficiency
Chronic (Painless) Thyroid
Chronic Eosinophilic Leukemia (CEL)
Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma
Chronic Myeloid Leukemia (CML)
Chronic Myelomonocytic Leukemia (CMML)
Chronic Neutrophilic Leukemia (CNL)
Citrullinemia (CIT1)
Classical Hodgkin Lymphoma (CHL)
Common Variable Immunodeficiency (CVID)
Congenital Adrenal Hyperplasia (CAH)
Congenital Adrenal Hyperplasia (CAH)
Coronary Artery Vasospasm
Crigler Najjar Disease
Cyclooxygenase (CO) Deficiency
Cystathionuria
Cystic Fibrosis (CF)
Decreased Serum Aldosterone
Decreased Urine Specific Gravity
Defects in Synthesis of Apolipoprotein A-I
Delta-Beta-Thalassemia
Delta-Thalassemia
Diabetes, Type I
Diabetes, Type II
Diffuse Large B-cell Lymphoma (DLBCL)
Diseases of the Glomeruli
Disseminated Intravascular Coagulation (DIC)
Disseminated Intravascular Coagulation (DIC)
Drug-Induced Hemolytic Anemia
Drug-Induced Hypothyroidism
Drug-Induced Neutropenia
Dubin Johnson syndrome
Eclampsia
Eclampsia
Ectopic ACTH syndrome (EAS)
Ectopic Thyroid Tissue
Elevated 24-Hour Urine Free Cortisol
Elevated Blood Lead Level
Elevated Hemoglobin and Hematocrit
Elevated Platelet Count
Elevated Serum Amylase and/or Serum Lipase
Elevated Serum Calcium
Elevated Serum or Plasma Potassium
Elevated Serum or Plasma Sodium
Elevated TSH – Hypothyroidism
Elevated WBC Count
Encephalitis
Essential Thrombocythemia
Factitious Hyperthyroidism
Factor V Deficiency – Congenital
Factor V Deficiency – Acquired
Factor V Leiden Mutation
Factor VII Deficiency – Acquired
Factor VII Deficiency – Congenital
Factor VIII Inhibitors in Patients with Congenital Factor VIII Deficiency
Factor VIII Inhibitors in Patients without Congenital Factor VIII Deficiency
Factor X Deficiency – Acquired
Factor X Deficiency – Congenital
Factor XI Deficiency – Acquired
Factor XI Deficiency – Congenital
Factor XII Deficiency – Acquired
Factor XII Deficiency – Congenital
Factor XIII Deficiency – Acquired
Factor XIII Deficiency – Congenital
Familial Apolipoprotein CII Deficiency
Familial Combined Hyperlipidemia (FCH)
Familial Defective Apolipoprotein B-100 (FDB)
Familial Dysbetalipoproteinemia
Familial Hyperalphalipoproteinemia
Familial Hypercholesterolemia (FH)
Familial Hypoalphalipoproteinemia
Familial Hypocalciuric Hypercalcemia
Familial Lipoprotein Lipase Deficiency
Fanconi Syndrome
Fibrinogen Deficiency – Acquired
Fibrinogen Deficiency – Congenital
Folate Deficiency
Follicular Lymphoma
Gastritis
Gastrointestinal (GI) Angiodysplasia
Gestational Diabetes
Gestational Thyrotoxicosis
Giant Cell (Temporal) Arteritis (GCA)
Gigantism
Gilbert's Disease
Gitelman's Syndrome
Glanzmann Thrombasthenia (GT)
HCG-Secreting Tumor
HELLP Syndrome
Hairy Cell Leukemia
Hashimoto's Disease
Heart Failure (HF)
Hemoglobinuria
Hemolytic Disease of the Newborn (HDN)
Hemolytic-Uremic Syndrome (HUS)
Hemophilia A (Factor VIII Deficiency) – Congenital
Hemophilia B (Factor IX Deficiency) – Acquired
Hemophilia B (Factor IX Deficiency) – Congenital
Hemostasis Defects Associated with Liver Disease
Hemostasis Defects Associated with Uremia
Hepatitis A Virus (HAV)
Hepatitis B Virus (HBV)
Hepatitis C Virus (HCV)
Hepatitis D (HDV)
Hepatitis E Virus (HEV)
Hepatitis G (GBV-C)
High Molecular Weight Kininogen Deficiency – Acquired
High Molecular Weight Kininogen Deficiency – Congenital
Homocystinuria
Hypercalcemia of Malignancy
Hyperglycemic Crisis
Hypergonadotropic Hypogonadism
Hypermethioninemia
Hyperprolactinemia Associated with Drugs
Hyperprolactinemia Associated with Hypothalamic Disorder
Hyperprolactinemia Associated with Pituitary Adenoma
Hypersensitivity Vasculitis
Hyperthyroidism: McCune Albright Syndrome (MAS)
Hypogonadotropic Hypogonadism (HH)
Hypothalamic Diabetes Insipidus (DI)
Hypothalamic Disease
INR Above or Below the Therapeutic Range
Idiopathic Aplastic Anemia
IgA Deficiency
IgG Subclass Deficiency
Increased Cardiovascular Risk
Increased D-Dimer or FDP
Increased Nitrates in the Urine
Increased PT Only: A Prolonged PT with a Normal PTT
Increased PT and Increased PTT
Increased Risk for Diabetes
Increased Serum Aldosterone
Increased Urinary Glucose
Increased Urinary Metanephrines
Increased Urinary Protein
Infectious Arthritis
Infective Endocarditis (IE)
Infertility
Infiltrative Thyroid Disorders
Intoxication with Ethanol
Intoxication with Isopropanol
Intoxication with Methanol
Iodine Deficiency
Iron Deficiency Anemia
Lambert-Eaton Myasthenic Syndrome (LEMS)
Large Intestine, Infection Protozoa
Large Intestine, Infection, Worms
Large Intestine, Infectious Diarrhea: Inpatient
Large Intestine, Infectious Diarrhea: Outpatient, Including Traveler’s Diarrhea
Large Intestine, Neoplastic: Adenocarcinoma
Lecithin Cholesterol Acyltransferase (LCAT) Deficiency
Liddle Syndrome
Lipodystrophy
Lipoprotein Syndromes, Primary/Non-Genetic
Liver, Failure
Low Hemoglobin or Hematocrit
Low Serum Calcium
Low Serum Cortisol
Low Serum or Plasma Glucose – Hypoglycemia
Low Serum or Plasma Potassium
Low Serum or Plasma Sodium
Low TSH – Hyperthyroidism
Low pO2 (Hypoxemia or Low O2 in Blood)
Lung Cancer
Lymphocyte-Depleted Classical Hodgkin Lymphoma (LDCHL)
Lymphocyte-Rich Classical Hodgkin Lymphoma (LRCHL)
Lymphocytosis
Lymphoid Interstitial Pneumonia (LIP)
Lymphomatoid Granulomatosis (LYG)
Lymphoplasmacytic Lymphoma
Male and Female Reproductive, Infectious Diseases (Sexually Transmitted Diseases; STDs)
Mantle Cell Lymphoma
Maple Syrup Urine Disease (MSUD)
Marginal zone lymphomas of mucosa-associated lymphoid tissue MALTomas
Menetriers Disease
Mercury Toxicity Levels in Humans
Metabolic Acidosis: Low Arterial pH and Low Arterial H2CO3-
Metabolic Alkalosis: Arterial Blood pH Elevated with Increased Arterial pCO2
Metabolic Syndrome
Milk-Alkali Syndrome
Mixed Cellularity Classical Hodgkin Lymphoma (MCCHL)
Monoclonal Protein on Serum Protein Electrophoresis (M Component)
Multiple Endocrine Neoplasia Syndromes: McCune Albright Syndrome
Multiple Endocrine Neoplasia Type 2A (MEN2A)
Multiple Endocrine Neoplasia Type 2B (MEN2B)
Multiple Endocrine Neoplasia Type I (MEN1)
Multiple Sclerosis
Myasthenia Gravis
Myelodysplastic Syndrome (MDS)
Myocarditits (Non-infectious)
N-acetylglutamate Synthase Deficiency
Nephrogenic Diabetes Insipidus
Nephrogenic Diabetes Insipidus
Nephrotic Syndrome
Neuroblastoma
Neutrophilia
Nodular Lymphocyte Predominant Hodgkin Lymphoma (NLPHL)
Nodular Sclerosis Classical Hodgkin Lymphoma (NSCHL)
Organophosphate Poisoning
Ornithine Transcarbamylase (OTC) Deficiency
Osteopenia/Osteoporosis
Osteopetrosis
Overdose of Amphetamine
Overdose of Barbiturate
Overdose of Benzodiazepine
Overdose of Cocaine
Overdose of Ethylene Glycol
Overdose of Gamma-Hydroxybutyrate (GHB)
Overdose of Opioid
Overdose of Propylene Glycol
Overdose of Tricyclic Antidepressant
Pancreatitis (ACUTE)
Paroxysmal Nocturnal Hemoglobinuria (PNH)
Pericarditis/Myocarditis, Infectious
Phenylketonuria (PKU)
Pheochromocytoma (PCC)
Plasma Cell Myeloma
Plasmablastic Lymphoma (PBL)
Plasminogen Deficiency
Platelet Function Disorder Produced by Aspirin
Platelet Function Disorder Produced by Glycoprotein IIb/IIIa Inhibitors
Platelet Function Disorder Produced by Plavix
Platelet Function Disorder Produced by Prasugrel
Platelet Storage Pool Disease – Congenital Alpha Granule Deficiency
Platelet Storage Pool Disease – Congenital Delta Granule Deficiency
Pneumonia – Atypical Organisms
Pneumonia, Infectious
Poisoning with Cyanide
Polyarteritis Nodosa (PAN)
Polycythemia Vera (PV)
Polycythemia Vera (PV)
Polyglandular Autoimmune (PGA) Syndrome
Porphyrias
Porphyrias
Positive Anti-Nuclear Antibody (ANA) Test
Positive Screening Test for HIV
Positive Serologic Test for
Positive Serologic Test for Hepatitis A Virus (HAV)
Positive Serologic Test for Hepatitis B Virus (HBV)
Positive Serologic Test for Hepatitis C Virus (HCV)
Post-ablative Hypothyroidism
Postpartum Thyroid Dysfunction
Postpartum Thyroiditis (PPT)
Precocious Puberty (PP)
Pregnancy-Related Infections
Prekallikrein Deficiency – Acquired
Prekallikrein Deficiency – Congenital
Premature Labor
Primary Aldosteronism (Conn's Syndrome)
Primary Amenorrhea due to Anatomical Defects
Primary Amenorrhea due to Enzymatic Deficiencies
Primary Amenorrhea due to Hypothalamic disease
Primary Amenorrhea due to Pituitary Disease
Primary Amenorrhea due to Polycystic Ovarian Syndrome (PCOS)
Primary Amenorrhea due to Premature Ovarian Failure (POF)
Primary Amenorrhea due to Pure Gonadal Dysgenesis/Agenesis
Primary Amenorrhea due to Turner Syndrome (TS)
Primary Cutaneous Anaplastic Large Cell Lymphoma
Primary Hypoaldosteronism
Primary Metabolic Osteomalacia
Primary Myelofibrosis (PMF)
Primary T-Cell Immunodeficiency: DiGeorge Syndrome
Prolonged PTT with a Normal PT
Prostate Cancer
Protein C Deficiency
Protein S Deficiency
Prothrombin (Factor II) Deficiency – Congenital
Prothrombin (Factor II) Deficiency – Acquired
Prothrombin 20210 Mutation
Pseudoaldosteronism
Pseudohypoaldosteronism (PHA)
Pseudohypoglycemia
Pseudohypoparathyroidism
Psychogenic Polydipsia
Pulmonary Alveolar Proteinosis (PAP)
Pyelonephritis caused by Escherichia Coli
Pyelonephritis caused by Klebsiella Spp.
Pyruvate Carboxylase Deficiency (PC)
Pyruvate Kinase Deficiency (PKD)
Renal Cell Carcinoma
Renal Disease Associated With Diabetes (Diabetes Nephropathy)
Respiratory Acidosis: Low Arterial Blood pH with Increased Arterial pCO2 and Arterial H2CO3- Increased
Respiratory Alkalosis: Arterial Blood pH Increased with Decreased Arterial pCO and Decreased Arterial H2CO3-
Respiratory Distress Syndrome (RDS)
Rheumatoid Arthritis (RA)
Rotor Syndrome
Scott Syndrome
Secondary Aldosteronism (Renovascular Hypertension)
Secondary Amenorrhea Associated with Cushings Syndrome
Secondary Amenorrhea Associated with Hypopituitarism
Secondary Amenorrhea Associated with Hypothyroidism
Secondary Amenorrhea Associated with Polycystic Ovarian Syndrome
Secondary Amenorrhea Associated with Pregnancy
Secondary Amenorrhea Associated with Prolactin-Secreting Pituitary Tumor
Secondary Hyperparathyroidism
Secondary Hypoaldosteronism (Hyporeninemic Hypoaldosteronism)
Secondary or Tertiary Adrenal Insufficiency
Sepsis and Bloodstream Infections
Severe Combined Immunodeficiency (SCID)
Sickle Cell Anemia
Sickle Cell Trait
Sjogrens Syndrome (SS)
Somogyi Phenomenon
Spontaneous Bacterial Peritonitis (SBP)
Subacute Thyroiditis
Syndrome of Inappropriate Antidiuretic Hormone Secretion
Systemic Lupus Erythematosus (SLE)
Systemic Lupus Erythematosus (SLE)
Systemic Sclerosis (SSc)
T-Cell Histiocyte Rich Large B-Cell Lymphoma (THRLB-CL)
TSH-Secreting Pituitary Adenoma
Tangier Disease
Thrombotic Thrombocytopenic Purpura (TTP)
Thromboxane Receptor Deficiency
Thromboxane Synthetase Deficiency
Thyroid Cancer (TC)
Thyroid Stimulating Hormone (TSH) Deficiency
Thyroiditis – Hashimoto's, Post Partum, Sub Acute and Atrophic
Toxic Adenoma
Toxic Multinodular Goiter (TMG)
Toxicity Associated with Acetaminophen
Toxicity Associated with Arsenic
Toxicity Associated with Carbon Monoxide
Toxicity Associated with Iron
Toxicity Associated with Lead
Toxicity Associated with Salicylate/Reye Syndrome
Transitional Cell Carcinoma
Tuberculosis
Tyrosinemia
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