Pharma Intelligence Disease Hub
Coverage of 891 BMT indications and counting...
Biomedtracker & Datamonitor Healthcare Joint Disease Coverage
198 diseases jointly covered in Biomedtracker and Datamonitor Healthcare. For a full list of Biomedtracker diseases click the Biomedtracker Diseases menu above.
ALLERGY
AUTOIMMUNE/IMMUNOLOGY
Acquired Hemophilia - Rare Disease
Activated PI3K Delta Syndrome (APDS) - Rare Disease
Anti-neutrophil Cytoplasmic Antibodies (ANCA) Associated Vasculitis - Rare Disease
Anti-synthetase syndrome (ASyS) - Rare Disease
Antibody Mediated Rejection (AMR)
Autoimmune Hepatitis - Rare Disease
Autoimmune Inner Ear Disease (AIED)
Behçet Syndrome - Rare Disease
Bone Marrow and Stem Cell Transplant - Graft vs. Host Disease (GVHD) Prophylaxis - Rare Disease
Bullous Pemphigoid - Rare Disease
Castleman's Disease - Rare Disease
CHAPLE Syndrome - Rare Disease
Chronic Fatigue Syndrome (CFS)
Chronic Granulomatous Disease - Rare Disease
Complement Deficiencies / Abnormalities
Cryoglobulinemia - Rare Disease
Cryopyrin (CIAS1)-Associated Periodic Syndromes (CAPS) - Rare Disease
CTLA-4 Deficiency - Rare Disease
Cutaneous Lupus Erythematosus (CLE) - Rare Disease
Dermatomyositis - Rare Disease
DiGeorge Syndrome - Rare Disease
Eosinophilic Esophagitis (EoE) - Rare Disease
Generalized Pustular Psoriasis (GPP) - Rare Disease
Giant Cell Arteritis - Rare Disease
Graft vs. Host Disease (GVHD) - Treatment - Rare Disease
Guillain-Barré Syndrome - Rare Disease
Hemolytic Disease of the Newborn (HDN)
Hereditary Angioedema (HAE) - Rare Disease
Idiopathic CD4+ Lymphocytopenia
IgM Neuropathy - Rare Disease
Immune Thrombocytopenic Purpura (ITP) - Rare Disease
Immunoglobulin-A (IgA) Deficiency
Inflammatory Bowel Disease (IBD)
Juvenile Idiopathic Arthritis - Rare Disease
Kawasaki Disease - Rare Disease
Lambert-Eaton Myasthenic Syndrome (LEMS) - Rare Disease
Lupus Nephritis - Rare Disease
Mast Cell Activation Syndrome (MCAS) - Rare Disease
Mastocytosis - Rare Disease
Myasthenia Gravis (MG) - Rare Disease
Nakajo-Nishimura Syndrome - Rare Disease
Palmoplantar Pustulosis (PPP) - Rare Disease
Paroxysmal Nocturnal Hemoglobinuria (PNH) - Rare Disease
Pemphigus Vulgaris - Rare Disease
Polymyositis - Rare Disease
Primary Biliary Cholangitis (PBC) - Rare Disease
Primary Sclerosing Cholangitis (PSC) - Rare Disease
Pyoderma Gangrenosum - Rare Disease
Rheumatoid Arthritis - Imaging
Sarcoidosis - Rare Disease
Scleroderma - Rare Disease
Sjogren's Disease - Rare Disease
Small Bowel Transplant Rejection
Sporadic Inclusion Body Myositis (sIBM) - Rare Disease
Systemic Lupus Erythematosus (SLE) - Rare Disease
Systemic Sclerosis - Rare Disease
Systemic Sclerosis-Associated Interstitial Lung Disease (SSc-ILD) - Rare Disease
Tumor Necrosis Factor (TNF) Receptor-Associated Periodic Syndrome (TRAPS) - Rare Disease
CARDIOVASCULAR
Acute Decompensated Heart Failure - Preserved Ejection Fraction (Acute HFpEF)
Acute Decompensated Heart Failure - Reduced Ejection Fraction (Acute HFrEF)
Acute heart failure - unspecified ejection fraction
Buerger's Disease - Rare Disease
Cardiomyopathy - Dilated - Rare Disease
Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT) - Rare Disease
Chronic Heart Failure - Preserved Ejection Fraction (Chronic HFpEF)
Chronic Heart Failure - Reduced Ejection Fraction (Chronic HFrEF)
Chronic Heart Failure and Cardiomyopathies - Unspecified
Congenital Heart (Cardiac) Defects
Coronary Artery Bypass Graft (CABG)
Coronary Artery Disease – Imaging
Dyslipidemia / Hypercholesterolemia
Heparin-Induced Thrombocytopenia (HIT)
Heterozygous Familial Hypercholesterolemia (HeFH)
Homozygous Familial Hypercholesterolemia (HoFH) - Rare Disease
Lymphatic Malformation (LM) - Rare Disease
Myocarditis (inflammatory cardiomyopathy)
Orthostatic Hypotension - Rare Disease
Patent Ductus Arteriosus (PDA) - Rare Disease
Percutaneous Coronary Intervention Restenosis
Percutaneous Coronary Interventions (PCIs) for Stable Angina
Peripheral Arterial Disease (PAD)
Portal Hypertension - Rare Disease
Pulmonary Arterial Hypertension (PAH) and Pulmonary Hypertension (PH) - Rare Disease
Supraventricular Tachycardia - Rare Disease
DERMATOLOGY
Congenital Ichthyosis - Rare Disease
Female Pattern Hair Loss (FPHL)
Gougerot-Carteaud Syndrome (Confluent and Reticulated Papillomatosis (CARP)) - Rare Disease
Hidradenitis Suppurativa - Rare Disease
Hypertrophic and Other Scarring - Rare Disease
ENDOCRINE
Achondroplasia - Rare Disease
Acromegaly - Rare Disease
Alcoholic Liver Disease / Alcoholic Hepatitis
Bone Complications (Including Bone Metastases)
Central Diabetes Insipidus (CDI)
Congenital Adrenal Hyperplasia (CAH) - Rare Disease
Congenital Hyperinsulinism (CHI) - Rare Disease
Cushing's Syndrome - Rare Disease
Diabetic Foot and Other Ulcers
Growth Hormone Insensitivity Syndrome (GHIS) - Rare Disease
Hepatorenal Syndrome (HRS) - Rare Disease
Hyperparathyroidism - Imaging - Rare Disease
Hyperthyroidism / Graves' Disease
Hypochondroplasia - Rare Disease
Hypoparathyroidism - Rare Disease
Hypophosphatasia - Rare Disease
McCune-Albright Syndrome - Rare Disease
Metabolic Dysfunction-Associated Steatohepatitis (MASH) - Imaging
Nephrogenic Diabetes Insipidus (NDI)
Osteogenesis Imperfecta (OI) - Rare Disease
Osteonecrosis - Rare Disease
Osteopetrosis - Rare Disease
Paget Disease of Bone - Rare Disease
Polyendocrine Metabolic Ovarian Syndrome (PMOS)
Prader-Willi Syndrome - Rare Disease
Primary Adrenal Insufficiency (Addison's Disease) - Rare Disease
Primary Hyperparathyroidism - Rare Disease
Secondary Hyperparathyroidism - Rare Disease
Short Stature / Growth Hormone Deficiency - Rare Disease
Turner Syndrome - Rare Disease
ENT/DENTAL
Meniere's Disease - Rare Disease
Otoferlin Gene-Mediated Hearing Loss - Rare Disease
GASTROENTEROLOGY (NON INFLAMMATORY BOWEL DISEASE)
Gastroesophageal Reflux Disease (GERD)
Hirschsprung's Disease - Rare Disease
Liver Failure / Cirrhosis - Rare Disease
Low Anterior Resection Syndrome
Microvillus Inclusion Disease (MVID) - Rare Disease
Necrotizing Enterocolitis (NEC) - Rare Disease
Opioid Induced Constipation (OIC)
Short Bowel Syndrome (SBS) - Rare Disease
HEMATOLOGY
Anemia Due to Chronic Kidney Disease, Dialysis-Dependent
Anemia Due to Chronic Kidney Disease, Dialysis-Independent
Aplastic Anemia - Rare Disease
Autoimmune Hemolytic Anemia (AIHA) - Rare Disease
Clonal Cytopenia of Undetermined Significance (CCUS) - Rare Disease
Congenital Megakaryocytic Thrombocytopenia - Rare Disease
Factor X (Stuart-Prower Factor) Deficiency - Rare Disease
Factor XIII Deficiency - Rare Disease
Fanconi Anemia - Rare Disease
Glanzmann Thrombasthenia - Rare Disease
Hemolytic Uremic Syndrome (HUS) - Rare Disease
Hemophilia A - Rare Disease
Hemophilia A and B - General Clotting Products - Rare Disease
Hemophilia B - Rare Disease
Iron Overload - Rare Disease
Sickle Cell Disease - Rare Disease
Sinusoidal Obstruction Syndrome (Veno-Occlusive Disease / VOD) - Rare Disease
Stroke Prevention in Atrial Fibrillation (SPAF)
Thalassemia - Rare Disease
Thrombotic Thrombocytopenic Purpura (TTP) - Rare Disease
Transplant-Associated Thrombotic Microangiopathy (TA-TMA)
Von Willebrand Disease - Rare Disease
Wiskott-Aldrich Syndrome - Rare Disease
INFECTIOUS DISEASE
Anthrax Infection - Rare Disease
Anti-Parasitic and Anti-Protozoal
Antibacterial and Antifungal - Miscellaneous Vaccines and Treatments
Antiviral - Miscellaneous Vaccines
Aspergillosis - Rare Disease
Bacterial Skin and Skin-Structure Infections
Chickenpox and Shingles - Vaccines and Treatments
Chikungunya Virus - Rare Disease
Clostridium difficile-Associated Diarrhea/Infection (CDAD/CDI)
Community Acquired Pneumonia (CAP)
Cryptococcosis - Rare Disease
Cytomegalovirus (CMV) Infection
Dengue Fever - Vaccines and Treatments
Diphtheria, pertussis, and tetanus (DT, Td, DTaP and Tdap) Vaccines - Rare Disease
Ebola - Rare Disease
Hepatitis D (HDV) Treatment - Rare Disease
Hepatitis E (HEV) Treatment - Rare Disease
Herpetic Keratitis - Rare Disease
Hib vaccines (Haemophilus influenzae b) - Rare Disease
Hospital Acquired (Nosocomial) Pneumonia (HAP)
Human papillomavirus (HPV) Prevention
Human Papillomavirus (HPV) Treatment
Influenza (excluding vaccines)
Influenza (including vaccines)
Japanese Encephalitis - Rare Disease
Leishmaniasis - Rare Disease
Leprosy - Rare Disease
Malaria - Rare Disease
Marburg Hemorrhagic Fever - Rare Disease
Measles, Mumps and Rubella (MMR) Vaccines - Rare Disease
Meningococcal Vaccines and Other Meningococcus-Specific Agents - Rare Disease
Non-Tuberculous Mycobacteria (NTM) - Rare Disease
Periprosthetic Joint Infection (PJI) - Rare Disease
Pertussis (Whooping Cough) - Rare Disease
Pneumococcal (Streptococcus pneumoniae) Vaccines
Pneumocystis carinii Pneumonia (PCP)
Poliovirus vaccines - Rare Disease
Progressive Multifocal Leukoencephalopathy (PML) - Rare Disease
Rabies - Rare Disease
Respiratory Papillomatosis (RP)
Respiratory Syncytial Virus (RSV) Prevention
Respiratory Syncytial Virus (RSV) Treatment
Respiratory Tract Infections (Excluding Pneumonia)
Septicemia or Bacteremia (including Endocarditis)
Severe Acute Respiratory Syndrome (SARS)
Smallpox - Rare Disease
Staphylococcal Vaccines and Other Staphylococcus-Specific Agents
Tuberculosis - Rare Disease
Urinary Tract and Reproductive Tract Infections
West Nile Virus - Rare Disease
Yellow Fever - Rare Disease
Zika Virus Disease - Rare Disease
METABOLIC
Aceruloplasminemia - Rare Disease
Acid Sphingomyelinase Deficiency (ASMD) - Rare Disease
Adrenoleukodystrophy - Rare Disease
Alagille Syndrome - Rare Disease
Alkaptonuria - Rare Disease
Alpha-1 Antitrypsin Deficiency (A1AD or AATD) - Rare Disease
Alpha-mannosidosis - Rare Disease
Amyloid light-chain (AL) Amyloidosis - Rare Disease
Amyloidosis - Rare Disease
Autosomal dominant hypocalcemia with hypercalciuria (ADHH) - Rare Disease
Becker Muscular Dystrophy (BMD) - Rare Disease
Biotin Thiamine Responsive Basal Ganglia Disease (BTBGD) - Rare Disease
Centronuclear Myopathies (CNMs) - Rare Disease
Cerebrotendinous Xanthomatosis (Cerebral Cholesterosis) - Rare Disease
Cockayne Syndrome (Weber-Cockayne / Neill-Dingwall Syndrome) - Rare Disease
Congenital Muscular Dystrophy (CMD) - Rare Disease
Congenital Sucrase-Isomaltase Deficiency (CSID) - Rare Disease
Crigler-Najjar Syndrome - Rare Disease
Cystinosis - Rare Disease
Cystinuria - Rare Disease
Danon Disease - Rare Disease
Disorders in Bile Acid Synthesis - Rare Disease
Duchenne Muscular Dystrophy (DMD) - Rare Disease
Epidermolysis Bullosa - Rare Disease
Fabry's Disease - Rare Disease
Facioscapulohumeral Muscular Dystrophy (FSHD) - Rare Disease
Familial Chylomicronemia Syndrome (FCS)/Lipoprotein Lipase Deficiency (LPLD) - Rare Disease
Familial Partial Lipodystrophy (FPL) - Rare Disease
Farber Disease - Rare Disease
Fatty Acid Oxidation Disorders (FAOD)
Fibrodysplasia Ossificans Progressiva (FOP) - Rare Disease
Galactosialidosis - Rare Disease
Gaucher's Disease - Rare Disease
Glycogen Storage Disease (GSD) - Rare Disease
GM1 Gangliosidosis - Rare Disease
GM2 Gangliosidoses (Tay-Sachs Disease, Sandhoff Disease, AB Variant) - Rare Disease
GNE-Related Myopathy (Inclusion Body Myopathy 2) - Rare Disease
Hereditary Hemorrhagic Telangiectasia (HHT, Osler–Weber–Rendu disease) - Rare Disease
Hereditary Transthyretin (hATTR) Amyloidosis With Polyneuropathy (Familial Amyloid Polyneuropathy) - Rare Disease
Hermansky-Pudlak syndrome (HPS)
Homocystinuria - Rare Disease
Hutchinson–Gilford Progeria Syndrome - Rare Disease
Hyperammonemia - Rare Disease
Hypohidrotic Ectodermal Dysplasia - Rare Disease
Hypoplasminogenemia - Rare Disease
Krabbe Disease (Globoid Cell Leukodystrophy) - Rare Disease
LCAT Deficiency - Rare Disease
Leigh's Disease - Rare Disease
Limb-Girdle Muscular Dystrophy (LGMD) - Rare Disease
Lipodystrophy - Rare Disease
Lysosomal Acid Lipase Deficiency - Rare Disease
Maple Syrup Urine Disease - Rare Disease
Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCADD) - Rare Disease
Metachromatic Leukodystrophy - Rare Disease
Mitochondrial Respiratory-Chain Diseases - Rare Disease
Molybdenum Cofactor Deficiency (MoCD) - Rare Disease
Mucolipidosis Type IV (MLIV) - Rare Disease
Mucopolysaccharidosis I (MPS I; Hurler Syndrome) - Rare Disease
Mucopolysaccharidosis II (MPS II; Hunter Syndrome) - Rare Disease
Mucopolysaccharidosis III - Subtype Undisclosed (MPS III; Sanfilippo Syndrome) - Rare Disease
Mucopolysaccharidosis IIIA (MPS IIIA; Sanfilippo A Syndrome) - Rare Disease
Mucopolysaccharidosis IIIB (MPS IIIB; Sanfilippo B Syndrome) - Rare Disease
Mucopolysaccharidosis IV (MPS IV; Morquio Syndrome) - Rare Disease
Mucopolysaccharidosis VI (MPS VI) - Rare Disease
Mucopolysaccharidosis VII (MPS VII; Sly Syndrome) - Rare Disease
Multiple Epiphyseal Dysplasia (MED)
Muscular Dystrophy - Unspecified - Rare Disease
Myotonic Muscular Dystrophy - Rare Disease
Neuronal Ceroid Lipofuscinosis (NCL) - Rare Disease
Niemann-Pick Disease Type C - Rare Disease
Noonan Syndrome - Rare Disease
Oculopharyngeal Muscular Dystrophy (OPMD) - Rare Disease
Organic Acidemias - Methylmalonic Acidemia (MMA) and Others - Rare Disease
Ornithine Transcarbamylase (OTC) Deficiency - Rare Disease
Pantothenate Kinase-associated Neurodegeneration (PKAN) - Rare Disease
Pelizaeus-Merzbacher Disease (PMD) - Rare Disease
Phelan-McDermid Syndrome (PMS) - Rare Disease
Phenylketonuria (PKU) - Rare Disease
Pompe Disease - Rare Disease
Porphyria - Rare Disease
Primary Mitochondrial Myopathies (PMM) - Rare Disease
Progressive Familial Intrahepatic Cholestasis (PFIC) - Rare Disease
Proteus Syndrome - Rare Disease
Pyruvate Kinase Deficiency - Rare Disease
Smith-Magenis Syndrome - Rare Disease
Spinal Bulbar Muscular Atrophy (SBMA, Kennedy's Disease, X-linked spinal muscular atrophy type 1) - Rare Disease
Spinal Muscular Atrophy - Rare Disease
Transthyretin Amyloid Cardiomyopathy (ATTR-CM, Wild Type Or Hereditary) - Rare Disease
Urea Cycle Disorders and Derangements (UCD)
Weight Gain from Antipsychotic Use
Werner Syndrome - Rare Disease
Wilson's Disease - Rare Disease
X-Linked Hypophosphatemia (XLH) - Rare Disease
X-linked Myotubular Myopathy - Rare Disease
NEUROLOGY
Age-Associated Memory Impairment
Amyotrophic Lateral Sclerosis (ALS) - Rare Disease
Angelman Syndrome - Rare Disease
Ataxia Telangiectasia - Rare Disease
Autism Spectrum Disorders (Autism)
CDKL5 Deficiency Disorder (CDD) - Rare Disease
Cervical Dystonia - Rare Disease
Charcot-Marie-Tooth Disease - Rare Disease
Chemotherapy Induced Peripheral Neuropathy (CIPN)
Childhood-Onset Neurodegeneration with Brain Atrophy (CONDBA) - Rare Disease
Chronic Inflammatory Demyelinating Polyneuropathy (CIDP) - Rare Disease
Complex Regional Pain Syndrome (CRPS) - Rare Disease
Congenital Myasthenic Syndrome (CMS) - Rare Disease
Diabetic Peripheral Neuropathy (DPN)
Dravet Syndrome - Rare Disease
Essential Tremor - Rare Disease
Excessive Sleepiness Associated with Medical Conditions
Fragile X Syndrome - Rare Disease
Friedreich's Ataxia - Rare Disease
Frontotemporal Dementia (FTD) - Rare Disease
Hemorrhagic Stroke / Intracerebral Hemorrhage (ICH)
HIV-Associated Distal Sensory Polyneuropathy (HIV-DSP)
Huntington's Disease - Rare Disease
Infantile Spasms (West Syndrome) - Rare Disease
Lennox-Gastaut Syndrome (LGS) - Rare Disease
Leptomeningeal Disease (LMD) - Rare Disease
Levodopa-Induced Dyskinesia - Rare Disease
MELAS (Mitochondrial Encephalopathy Lactic Acidosis With Stroke-Like Episodes) - Rare Disease
Mild Cognitive Impairment (MCI)
Multifocal Motor Neuropathy (MMN) - Rare Disease
Multiple System Atrophy (MSA) - Rare Disease
Myelin Oligodendrocyte Glycoprotein Antibody-associated Disease (MOGAD) - Rare Disease
Narcolepsy - Rare Disease
Neonatal Seizures - Rare Disease
Neurofibromatosis (NF) - Rare Disease
Neuromuscular Spasm and Spasticity
Neuromyelitis Optica (Devic's Syndrome, NMO) - Rare Disease
Non-24 Hour Sleep Wake Disorder (Non-24) - Rare Disease
Parkinson's Disease Dementia (PDD)
Pontocerebellar Hypoplasia - Rare Disease
Postherpetic Neuralgia (PHN) - Rare Disease
Progressive Supranuclear Palsy - Rare Disease
Rett Syndrome - Rare Disease
Shift Work Sleep Disorder (SWSD)
Speech Impediment (Stuttering)
Spinal Cord Injury (SCI) - Rare Disease
Spinocerebellar Ataxia - Rare Disease
Tardive Dyskinesia - Rare Disease
Trigeminal Neuralgia - Rare Disease
NOT SPECIFIED
Acute Radiation Syndrome (ARS) - Rare Disease
OBSTETRICS/GYNECOLOGY
Asherman's Syndrome - Rare Disease
Eclampsia/Pre-Eclampsia - Rare Disease
ONCOLOGY
Acute Lymphoblastic Leukemia (ALL) - Rare Disease
Acute Myelogenous Leukemia (AML) - Rare Disease
Acute Promyelocytic Leukemia (APL) - Rare Disease
Adenoid Cystic Carcinoma (ACC) - Rare Disease
Adrenocortical Cancer - Rare Disease
Adult T-cell Leukemia/Lymphoma (ATL) - Rare Disease
Alveolar Soft Part Sarcoma (ASPS) - Rare Disease
Anal Cancer - Rare Disease
Anaplastic Large Cell Lymphoma (ALCL) - Rare Disease
Angioimmunoblastic T-Cell Lymphoma (AITL) - Rare Disease
Angiosarcoma - Rare Disease
Biliary Tract Cancer - Rare Disease
Blastic Plasmacytoid Dendritic Cell Neoplasm (BPDCN) - Rare Disease
Bone Cancer - General - Rare Disease
Bone Marrow Transplant and Stem Cell Transplant
Brain Cancer (Malignant Glioma; AA and glioblastoma) - Rare Disease
Brain Cancer (Secondary; Metastases)
Burkitt Lymphoma/Burkitt Leukemia - Rare Disease
Carcinoid Syndrome - Rare Disease
Cervical Cancer - Rare Disease
Chemotherapy Induced Nausea and Vomiting (CINV)
Chondrosarcoma - Rare Disease
Chronic Lymphocytic Leukemia (CLL)/Small Cell Lymphocytic Lymphoma (SLL) - Rare Disease
Chronic Myelogenous Leukemia (CML) - Rare Disease
Chronic Myelomonocytic Leukemia (CMML) - Rare Disease
Colorectal Cancer (CRC) - Imaging
Colorectal Liver Metastases (CRLM)
Cutaneous T-Cell Lymphoma (CTCL) - NHL - Rare Disease
Dermatofibrosarcoma Protuberans (DFSP) - Rare Disease
Desmoid Tumors - Rare Disease
Diffuse Large B-Cell Lymphoma (DLBCL) - Rare Disease
Epithelioid Sarcoma - Rare Disease
Esophageal Cancer - Rare Disease
Essential Thrombocythemia (ET) - Rare Disease
Ewing Sarcoma - Rare Disease
Familial Adenomatous Polyposis (FAP) - Rare Disease
Follicular Lymphoma (FL) - Rare Disease
Gastrointestinal Stromal Tumor (GIST) - Rare Disease
Germ Cell tumors (GCT) - Rare Disease
Hairy Cell Leukemia - Rare Disease
Head and Neck Cancer - Imaging
Hepatocellular (Liver) Cancer (HCC) (Including Secondary Metastases) - Rare Disease
Hepatocellular (Liver) Cancer (HCC) - Imaging
Histiocytosis - Rare Disease
Hodgkin's Lymphoma - Rare Disease
Hypereosinophilic Syndrome (HES) - Rare Disease
Indolent Non-Hodgkin's Lymphoma - iNHL
Kaposi's Sarcoma - Rare Disease
Leiomyosarcoma - Rare Disease
Li-Fraumeni Syndrome - Rare Disease
Liposarcoma - Rare Disease
Mantle Cell Lymphoma (MCL) - Rare Disease
Marginal Zone Lymphoma (MZL) - Rare Disease
Merkel Cell Carcinoma - Rare Disease
Mesothelioma - Rare Disease
Multiple Myeloma (MM) - Rare Disease
Myelodysplastic Syndrome (MDS) - Rare Disease
Myelofibrosis (MF) - Rare Disease
Myeloproliferative Disorders (MPD) - Rare Disease
Nasopharyngeal Cancer - Rare Disease
Neuroblastoma - Rare Disease
Neuroendocrine Tumors (NET) - Rare Disease
Non-Small Cell Lung Cancer (NSCLC)
Non-Small Cell Lung Cancer (NSCLC) - Imaging
Oral Leukoplakia - Rare Disease
Osteosarcoma - Rare Disease
Ovarian Cancer - Rare Disease
Pancreatic Cancer - Rare Disease
Peripheral T-Cell Lymphoma (PTCL) - Rare Disease
Polycythemia Vera (PV) - Rare Disease
Primary Central Nervous System Lymphoma (PCNSL) - Rare Disease
Prostatic Intraepithelial Neoplasia (PIN)
Renal Cell Cancer (RCC) - Rare Disease
Renal Cell Cancer (RCC) - Imaging
Rhabdomyosarcoma - Rare Disease
Schwannoma - Rare Disease
Secondary Central Nervous System Lymphoma (SCNSL) - Rare Disease
Skin Cancer - Basal Cell Carcinoma (BCC)
Skin Cancer - Basal Cell Carcinoma Nevus Syndrome (BCCNS) / Gorlin Syndrome - Rare Disease
Skin Cancer - Squamous Cell Carcinoma (SCC)
Small Cell Lung Cancer (SCLC) - Rare Disease
Soft Tissue Sarcoma - General - Rare Disease
Synovial Sarcoma - Rare Disease
Tenosynovial Giant Cell Tumor (TGCT) / Pigmented Villonodular Synovitis (PVNS) - Rare Disease
Testicular Cancer - Rare Disease
Thymic Carcinoma - Rare Disease
Thyroid Cancer - Rare Disease
Triple-Negative Breast Cancer (TNBC)
Tuberous Sclerosis Complex (TSC) - Rare Disease
Uterine (Endometrial) Cancer - Rare Disease
Uterine (Endometrial) Cancer - Imaging
Uveal Melanoma - Rare Disease
Von Hippel–Lindau (VHL) Disease - Rare Disease
Waldenstrom Macroglobulinemia (WM) / Lymphoplasmacytic Lymphoma (LPL) - Rare Disease
Zollinger-Ellison Syndrome - Rare Disease
OPHTHALMOLOGY
Achromatopsia - Rare Disease
Choroideremia - Rare Disease
Dry Age-Related Macular Degeneration (Dry AMD)/Geographic Atrophy
Glaucoma / Ocular Hypertension
Keratoconus - Rare Disease
Leber's Congenital Amaurosis - Rare Disease
Leber's Hereditary Optic Neuropathy (LHON) - Rare Disease
Macular Edema from Retinal Vein Occlusion (RVO)
Macular Neovascularization (MNV)
Macular Telangiectasia - Rare Disease
Myopic Macular Degeneration (MMD)/Pathological Myopia
Neovascular (Wet) Age-Related Macular Degeneration (nAMD)
Neurotrophic Keratopathy - Rare Disease
Ocular Pain and/or Inflammation
Ophthalmia Neonatorum (Neonatal Conjunctivitis)
Optic Neuritis - Rare Disease
Other Congenital Blindness Indications
Other Ophthalmological Indications
Proliferative Vitreoretinopathy (PVR) - Rare Disease
Retinitis Pigmentosa (RP) - Rare Disease
Retinopathy of Prematurity (ROP) - Rare Disease
Rhegmatogenous Retinal Detachment (RRD)
Stargardt Disease - Rare Disease
Usher Syndrome - Rare Disease
Uveitis - Rare Disease
X-Linked Retinoschisis - Rare Disease
ORTHOPEDICS
PSYCHIATRY
Antipsychotics - Revenue From Other Indications
Attention Deficit Hyperactivity Disorder (ADHD)
RENAL
Acute Kidney Injury (AKI)/Acute Renal Failure (ARF)
Alport Syndrome - Rare Disease
C3 Glomerulopathy (C3G), including Dense Deposit Disease (DDD) and C3 Glomerulonephritis (C3GN) - Rare Disease
End-Stage Renal Disease (ESRD)
Focal Segmental Glomerulosclerosis (FSGS) - Rare Disease
Hyperoxaluria - Rare Disease
Immunoglobulin A (IgA) Nephropathy (Berger's Disease) - Rare Disease
RESPIRATORY
Acute Respiratory Failure, Acute Lung Injury (ALI), Acute Respiratory Distress Syndrome (ARDS) - Rare Disease
Bronchiectasis - Rare Disease
Bronchopulmonary Dysplasia (BPD) - Rare Disease
Chronic Obstructive Pulmonary Disease (COPD)
Cystic Fibrosis (CF) - Rare Disease
Idiopathic Pulmonary Fibrosis (IPF) - Rare Disease
Pulmonary Alveolar Proteinosis (PAP) - Rare Disease