|
| Secondary failure reasons for the native organ. |
| May contain organization-specific values: Yes |
| Category Entries: |
| Allergic Bronchopulmonary Aspergillosis |
| Bronchopulmonary Dysplasia |
| Ciliary Dyskinesis Syndrome |
| Constrictive Bronchiolitis |
| Dysmotile Cilia Syndrome |
| Granulomatous Lung Disease |
| Kartagener's Syndrome |
| Obstructive Lung Disease |
| Primary Ciliary Dyskinesia |
| Tuberous Sclerosis |
| Congenital Malformation |
| Peripheral Pulm Artery Stenosis and Second Degree Pulm Htn |
| Portopulmonary Hypertension |
| Pulmonary AV Malformation Congenital Heart Disease |
| Pulmonary Thromboembolic Disease |
| Pulmonary Veno-Occlusive Disease |
| Pulmonic Stenosis |
| Right Hypoplastic Lung |
| Thromboembolic Pulmonary Hypertension |
| Wegener's Granuloma - Restrictive |
| Wegener's Granuloma - Bronchiectasis |
| Crest - Restrictive |
| Crest - Pulmonary Hypertension |
| Pulmonary Telangiectasia - Restrictive |
| Pulmonary Telangiectasia - Pulmonary Hypertension |
| Scleroderma - Restrictive |
| Scleroderma - Pulmonary Hypertension |
| Common Variable Immune Deficiency |
| Fibrocavitary Lung Disease |
| Hypogammaglobulinemia |
| Shwachman-Diamond Syndrome |
| Alveolar Proteinosis |
| Amyloidosis |
| ARDS/Pneumonia |
| IIP: BOOP/COP |
| Bronchoalveolar Carcinoma (BAC) |
| Carcinoid Tumorlets |
| Chronic Pneumonitis of Infancy |
| Collagen Vascular Diseases |
| Connective Tissue Disease |
| Crest |
| Cutis Laxa |
| Desquamative Interstitial Pneumonitis (DIP) |
| Ehlers-Danlos Syndrome |
| Eosinophilic Granuloma |
| Eosinophilic Granulomatosis |
| Eosinophilic Pneumonial Chronic Granulomatosis |
| Fibrosing Mediastinitis |
| Graft-Vs-Host Disease (GVHD) |
| Hermansky Pudlak Syndrome |
| Histiocytosis X |
| Hypersensitivity Pneumonitis |
| Idiopathic Pulmonary Hemosiderosis |
| Interstitial Pneumonitis |
| IIP: Lymphocytic Interstitial Pneumonia |
| Lupus |
| Macleod Syndrome |
| Mixed Connective Tissue Disease |
| Paraneoplastic Pemphigus Associated Castleman's Disease |
| Polymyositis |
| Pulmonary Hyalinizing Granuloma |
| Pulmonary Langerhans Cell Granulomatosis |
| Pulmonary Telangiectasia |
| Restrictive Lung Disease |
| Scleroderma |
| Sjogren's Syndrome |
| Silicosis |
| Surfactant Protein B Deficiency |
| Swyer James Syndrome |
| Teratoma |
| Tracheopathia Osteoplastica |
| Usual Interstitial Pneumonitis |
| Wegener's Granuloma |
| Other, Specify |
| Dilated Myopathy: Idiopathic |
| Dilated Myopathy: Adriamycin |
| Dilated Myopathy: Post Partum |
| Dilated Myopathy: Familial |
| Dilated Myopathy: Myocarditis |
| Dilated Myopathy: Alcoholic |
| Dilated Myopathy: Viral |
| Dilated Myopathy: Ischemic |
| Dilated Myopathy: Viral (Not COVID-19) |
| COVID-19: Dilated Myopathy: Active Myocarditis |
| COVID-19: Dilated Myopathy: History of Myocarditis |
| Dilated Myopathy: Other, Specify |
| Restrictive Myopathy: Idiopathic |
| Restrictive Myopathy: Amyloidosis |
| Restrictive Myopathy: Endocardial Fibros |
| Restrictive Myopathy: Sarcoidosis |
| Restrictive Myopathy: Sec to Radiat/Chem |
| Restrictive Myopathy: Other, Specify |
| Heart Re-Tx/Gf: Hyperacute Rejection |
| Heart Re-Tx/Gf: Acute Rejection |
| Heart Re-Tx/Gf: Coronary Artery Disease |
| Heart Re-Tx/Gf: Non-Specific |
| Heart Re-Tx/Gf: Restrictive/Constrictive |
| Heart Re-Tx/Gf: Chronic Rejection |
| Heart Re-Tx/Gf: Primary Failure |
| Heart Re-Tx/Gf: Other Specify |
| Coronary Artery Disease |
| Hypertrophic Cardiomyopathy |
| Valvular Heart Disease |
| Congenital Heart Defect - Prior Surgery Unknown |
| Cancer |
| Congenital Heart Defect - Hypoplastic Left Heart Syndrome - Unoperated |
| Congenital Heart Defect - Without Surgery |
| Congenital Heart Defect - With Surgery |
| Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy |
| Muscular Dystrophy: Other, Specify |
| Cardiac Disease: Other Specify |
| Heart: Other Specify |
| Eisenmenger's Syn: Atrial Septal Defect |
| Eisenmenger's Syn: VSD |
| Eisenmenger's Syn: PDA |
| Pulmonary Capillary Hemangiomatosis |
| ABCA3 Transporter Mutation |
| Secondary Pulmonary Fibrosis: Specify Cause |
| Surfactant Protein C Deficiency |
| IIP: Nonspecific Interstitial Pneumonia |
| IIP: Respiratory Bronchiolitis |
| IIP: Desquamative Interstitial Pneumonia |
| IIP: Acute Interstitial Pneumonia |
| Pulmonary Lymphangiectasia |
| Eisenmenger's Syn: Multi Congenital Anomalies |
| Eisenmenger's Syn: Other, Specify |
| Lung Re-Tx/Gf: Non-Specific |
| Lung Re-Tx/Gf: Obliterative Bronchiolitis |
| Lung Re-Tx/Gf: Restrictive |
| Lung Re-Tx/Gf: Acute Rejection |
| Lung Re-Tx/Gf: Obstructive |
| Lung Re-Tx/Gf: Primary Graft Failure |
| Lung Re-Tx/Gf: Obliterative Bronchiolitis-Restrictive |
| Lung Re-Tx/Gf: Obliterative Bronchiolitis-Obstructive |
| Lung Re-Tx/Gf: Other Specify |
| Congenital: Other Specify |
| Pulmonary Hypertension/Pulmonary Arterial Hypertension |
| Cystic Fibrosis |
| Inhalation Burns/Trauma |
| IIP: Idiopathic Pulmonary Fibrosis (IPF) |
| Sarcoidosis |
| Alpha - 1 - Antitrypsin Deficiency |
| COPD/Emphysema |
| Bronchiectasis |
| Rheumatoid Disease |
| Occupational Lung Disease Other, Specify |
| Lymphangioleiomyomatosis |
| Obliterative Bronchiolitis (Non-retransplant) |
| Pulmonary Fibrosis Other, Specify Cause |
| Pulmonary Vascular Disease |
| Secondary Pulmonary Hypertension |
| COVID-19: ARDS |
| COVID-19: Pulmonary Fibrosis |
| Combined Pulmonary Fibrosis and Emphysema (CPFE) |
| Heart/Lung Re-Tx/Gf: Primary Failure |
| Lung Disease: Other Specify |
| Idiopathic and Post-infectious Crescentic Glomerulonephritis |
| Membranous Glomerulonephritis |
| Mesangio-capillary Glomerulonephritis - Type I |
| Mesangio-capillary Glomerulonephritis Type II |
| IgA Nephropathy |
| Anti-GBM |
| Focal Glomerular Sclerosis (Focal Segmental - FSG) |
| Chronic Pyelonephritis (Reflux Nephropathy) |
| Polycystic Kidneys |
| Nephritis |
| Nephronophthisis |
| Diabetes - Type I Insulin Dep/Juvenile Onset |
| Diabetes - Type II Non-Insulin Dep/ Adult Onset |
| Oxalate Nephropathy (Includes Hereditary Oxalosis) |
| Cystinosis |
| Fabry's Disease |
| Amyloidosis - Kidney |
| Gout |
| Systemic Lupus Erythematosus |
| Progressive Systemic Sclerosis |
| Wilms' Tumor |
| Renal Cell Carcinoma |
| Incidental Carcinoma |
| Myeloma |
| Hemolytic Uremic Syndrome |
| Hypoplasia/Dysplasia/Dysgenesis/Agenesis |
| Cortical Necrosis |
| Acute Tubular Necrosis |
| Medullary Cystic Disease |
| Sickle Cell Anemia |
| Acquired Obstructive Nephropathy |
| Alport's Syndrome |
| Familial Nephropathy |
| Goodpasture's Syndrome |
| Malignant Hypertension |
| Henoch-Schonlein Purpura |
| Prune Belly Syndrome |
| Retransplant/Graft Failure Kidney |
| Diabetes - Type I Non-Insulin Dep/ Juvenile Onset |
| Diabetes - Type II Insulin Dep/Adult Onset |
| Hypertensive Nephrosclerosis |
| Chronic Glomerulonephritis - Unspecified |
| Membranous Nephropathy |
| Chronic Glomerulosclerosis - Unspecified |
| Analgesic Nephropathy |
| Radiation Nephritis |
| Antibiotic-Induced Nephritis |
| Cancer Chemotherapy Induced Nephritis |
| Calcineurin Inhibitor Nephrotoxicity |
| Heroin Nephrotoxicity |
| Renal Artery Thrombosis |
| Chronic Nephrosclerosis - Unspecified |
| Congenital Obstructive Uropathy |
| Scleroderma - Kidney |
| Wegener's Granulomatosis |
| Polyarteritis |
| Rheumatoid Arthritis |
| Sarcoidosis - Kidney |
| Lymphoma |
| Nephrolithiasis |
| Urolithiasis |
| Dysplasia |
| Pre-BMTransplantation Total Body Irradiation |
| Drug Related Interstitial Nephritis |
| Thin Basement Membrane Disease |
| Hereditary Oxalosis |
| Cholesterol Embolization |
| Focal Segmental Glomerulosclerosis |
| Rapid Progressive Glomerulonephritis (RPGN) |
| Diabetes Mellitus - Type I |
| Diabetes Mellitus - Type II |
| Diabetes Mellitus - Type Other / Unknown |
| Hepatorenal Syndrome |
| Lithium Toxicity |
| HIV Nephropathy |
| Acute Hepatic Necrosis (AHN): Drug, Specify |
| AHN: Type A |
| AHN: Type B, HBsAG+ |
| AHN: Non A, Non B |
| AHN: Type C |
| AHN: Type D |
| AHN: Type B and C |
| AHN: Type B and D |
| AHN: Etiology Unknown |
| AHN: Other, Specify |
| Cirrhosis: Drug or Industrial Exposure, Specify |
| Cirrhosis: Type A |
| Cirrhosis: Type B-, HBsAG+ |
| Cirrhosis: Non A, Non B |
| Cirrhosis: Type C |
| Cirrhosis: Type D |
| Cirrhosis: Type B and C |
| Cirrhosis: Type B and D |
| Cirrhosis: Cryptogenic-Idiopathic |
| Cirrhosis: Chronic Active Hepatitis: Etiology Unknown |
| Cirrhosis: Other, Specify |
| Cirrhosis: Autoimmune |
| Cirrhosis: Cryptogenic (Idiopathic) |
| Cirrhosis: Fatty Liver (NASH) |
| Alcoholic Cirrhosis |
| Alcoholic Cirrhosis with Hepatitis C |
| Acute Alcoholic Hepatitis |
| Acute Alcohol-Associated Hepatitis With or Without Cirrhosis |
| Alcohol-Associated Cirrhosis Without Acute Alcohol-Associated Hepatitis |
| Primary Biliary Cirrhosis (PBC) |
| Cirrhosis: Metabolic Dysfunction-Associated Steatohepatitis (MASH) |
| Cirrhosis: Metabolic Dysfunction and Alcohol-Related/Associated Liver Disease (MetALD) |
| Secondary Biliary Cirrhosis: Caroli's Disease |
| Secondary Biliary Cirrhosis: Choledochal Cyst |
| Secondary Biliary Cirrhosis: Other, Specify |
| Primary Sclerosing Cholangitis (PSC): Crohn's Disease |
| Primary Sclerosing Cholangitis: Ulcerative Colitis |
| Primary Sclerosing Cholangitis: No Bowel Disease |
| Primary Sclerosing Cholangitis: Other, Specify |
| Familial Cholestasis: Byler's Disease |
| Familial Cholestasis: Other, Specify |
| Cholestatic Liver Disease: Other, Specify |
| Neonatal Cholestatic Liver Disease |
| Neonatal Hepatitis, Specify |
| Biliary Atresia: Extrahepatic |
| Biliary Hypoplasia: Nonsyndromic Paucity of Intrahepatic Bile Duct |
| Biliary Hypoplasia: Alagille Syndrome (Paucity of Intrahepatic Bile Duct) |
| Biliary Atresia or Hypoplasia: Other, Specify |
| Congenital Hepatic Fibrosis |
| Cystic Fibrosis - Liver |
| Budd-Chiari Syndrome |
| Metabolic Disease (METDIS): Alpha-1-Antitrypsin Deficiency (A-1-A) |
| METDIS: Wilson's Disease, Other Copper Metabolism Disorder |
| METDIS: Hemochromatosis - Hemosiderosis |
| METDIS: Glycogen Storage Disease Type I (GSD-I) |
| METDIS: Glycogen Storage Disease Type IV (GSD-IV) |
| METDIS: Hyperlipidemia-II, Homozygous Hypercholesterolemia |
| METDIS: Tyrosinemia |
| METDIS: Primary Oxalosis/Oxaluria, Hyperoxaluria |
| METDIS: Maple Syrup Urine Disease |
| METDIS: Other, Specify |
| Primary Liver Malignancy: Hepatoma, Hepatocellular Carcinoma (HCC) |
| Primary Liver Malignancy: Hepatoma (HCC) and Cirrhosis |
| Primary Liver Malignancy: Fibrolamellar (FL-HC) |
| Primary Liver Malignancy: Cholangiocarcinoma (CH-CA) |
| Primary Liver Malignancy: Hepatoblastoma (HBL) |
| Primary Liver Malignancy: Hemangioendothelioma, Hemangiosarcoma, Angiosarcoma |
| Primary Liver Malignancy: Other, Specify |
| Bile Duct Cancer (Cholangioma, Biliary Tract Carcinoma) |
| Secondary Hepatic Malignancy: Specify |
| Benign Tumor: Hepatic Adenoma |
| Benign Tumor: Polycystic Liver Disease |
| Benign Tumor: Other, Specify |
| Total Parenteral Nutrition (TPN)/Hyperalimentation Induced Liver Disease |
| Graft vs. Host Disease Secondary to Non-Liver Transplant |
| Trauma, Specify |
| Hepatitis B: Chronic or Acute |
| Hepatitis C: Chronic or Acute |
| NA: Non-hd Followups Only |
| Graft Failure |
| Retransplant/Graft Failure Pancreas |
| Diabetes Mellitus - Type I (Pancreas) |
| Diabetes Mellitus - Type II (Pancreas) |
| Diabetes Secondary to Chronic Pancreatitis without Pancreatectomy |
| Diabetes Secondary to Cystic Fibrosis without Pancreatectomy |
| Pancreatic Cancer |
| Bile Duct Cancer |
| Other Cancers |
| Pancreatectomy Prior to Pancreas Transplant |
| Diabetes Mellitus - Type Other/Unknown (Pancreas) |
| SGS: Intestinal Atresia |
| SGS: Necrotizing Enterocolitis |
| SGS: Intestinal Volvulus Secondary to Malrotation |
| SGS: Intestinal Volvulus Secondary to Adhesions |
| SGS: Intestinal Volvulus Secondary to Persistent Omphalomesenteric Duct |
| SGS: Gastroschisis |
| SGS: Mass Resect Sec to Inflammatory Bowel Disease-Crohns |
| SGS: Mass Resect Sec to Tumor |
| SGS: Mass Resect Sec to Mesenteric Arterial Thrombosis or Embolus |
| SGS: Mass Resect Sec to Mesenteric Venous Thrombosis |
| SGS: Other Specify |
| SGS: Unspecified |
| FBP: Hirschsprung's Disease |
| FBP: Neuronal Intestinal Dysplasia |
| FBP: Pseudo-obstruction-Neuropathic |
| FBP: Pseudo-obstruction-Myopathic |
| FBP: Protein-losing Enteropathy |
| FBP: Microvillous Inclusion Disease |
| FBP: Other Specify |
| FBP: Unspecified |
| Graft Failure |
| Retransplant |
| Other Intestinal Disease, Specify |
| Trauma |
| Infection |
| Burn/explosion |
| Ischemia |
| Congenital |
| Malignancy |
| Metabolic |
