| Source | us.nlm.vsac#0.11.0:null (v4.0.1) |
| resourceType | ValueSet |
| id | 2.16.840.1.113883.17.4077.3.2062 |
| canonical | http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113883.17.4077.3.2062 |
| version | 20180226 |
| status | active |
| publisher | ACEP/AMA-PCPI Steward |
| name | OrganDysfunction |
| title | Organ Dysfunction |
| date | 2018-02-26T01:00:05-05:00 |
| experimental | false |
| Usages | (none) |
This value set contains 500 concepts
| Code | System | Display |
| 101301000119106 | http://snomed.info/sct | Acute hypercapnic respiratory failure due to obstructive sleep apnea (disorder) |
| 10153004 | http://snomed.info/sct | Systemic fibrinogenolysis (disorder) |
| 103931000119102 | http://snomed.info/sct | Hepatic coma due to hepatitis (disorder) |
| 105604006 | http://snomed.info/sct | Deficiency of naturally occurring coagulation factor inhibitor (disorder) |
| 1082621000119108 | http://snomed.info/sct | Hepatic coma due to alcoholic liver failure (disorder) |
| 1085091000119108 | http://snomed.info/sct | Hepatic coma due to chronic hepatic failure (disorder) |
| 1092691000119109 | http://snomed.info/sct | Hepatic coma due to subacute liver failure (disorder) |
| 10934005 | http://snomed.info/sct | Cryofibrinogenemia (disorder) |
| 111377009 | http://snomed.info/sct | Metabolic acidosis, normal anion gap (disorder) |
| 111452009 | http://snomed.info/sct | Postpartum afibrinogenemia with hemorrhage (disorder) |
| 111556005 | http://snomed.info/sct | Ketoacidosis without coma due to diabetes mellitus (disorder) |
| 111558006 | http://snomed.info/sct | Insulin coma (disorder) |
| 111588002 | http://snomed.info/sct | Heparin-induced thrombocytopenia with thrombosis (disorder) |
| 111589005 | http://snomed.info/sct | Dysfibrinogenemia (disorder) |
| 12153008 | http://snomed.info/sct | Acquired factor IX deficiency disease (disorder) |
| 12326000 | http://snomed.info/sct | Respiratory acidosis (disorder) |
| 123786007 | http://snomed.info/sct | Blood coagulation disorder with shortened coagulation time (disorder) |
| 123787003 | http://snomed.info/sct | Blood coagulation disorder with prolonged coagulation time (disorder) |
| 123788008 | http://snomed.info/sct | Blood coagulation disorder with shortened bleeding time (disorder) |
| 123789000 | http://snomed.info/sct | Blood coagulation disorder with prolonged bleeding time (disorder) |
| 123790009 | http://snomed.info/sct | Blood coagulation disorder with impaired clot retraction time (disorder) |
| 12546009 | http://snomed.info/sct | Hemorrhagic disease of the newborn due to vitamin K deficiency (disorder) |
| 125921000119106 | http://snomed.info/sct | Hepatic coma due to acute hepatitis C (disorder) |
| 127034005 | http://snomed.info/sct | Pancytopenia (disorder) |
| 128088003 | http://snomed.info/sct | Blood coagulation disorder, categorized by value of screening test (disorder) |
| 128090002 | http://snomed.info/sct | Benign gestational thrombocytopenia (disorder) |
| 128091003 | http://snomed.info/sct | Autoimmune thrombocytopenia (disorder) |
| 128092005 | http://snomed.info/sct | Secondary autoimmune thrombocytopenia (disorder) |
| 128093000 | http://snomed.info/sct | Alloimmune thrombocytopenia (disorder) |
| 128094006 | http://snomed.info/sct | Alloimmune platelet transfusion refractoriness (disorder) |
| 128105004 | http://snomed.info/sct | von Willebrand disorder (disorder) |
| 128106003 | http://snomed.info/sct | Hereditary von Willebrand disease type 1 (disorder) |
| 128107007 | http://snomed.info/sct | Hereditary von Willebrand disease type 2 (disorder) |
| 128108002 | http://snomed.info/sct | Hereditary von Willebrand disease type 3 (disorder) |
| 128113003 | http://snomed.info/sct | Hereditary von Willebrand disease type 1B (disorder) |
| 128114009 | http://snomed.info/sct | Hereditary von Willebrand disease type 1C (disorder) |
| 128115005 | http://snomed.info/sct | Pseudo von Willebrand disease (disorder) |
| 1286003 | http://snomed.info/sct | Vitamin K deficiency coagulation disorder (disorder) |
| 12983003 | http://snomed.info/sct | Failed attempted abortion with septic shock (disorder) |
| 13172003 | http://snomed.info/sct | Chronic idiopathic thrombocytopenic purpura (disorder) |
| 13507004 | http://snomed.info/sct | Purpura fulminans (disorder) |
| 13993001 | http://snomed.info/sct | Factor XIII inhibitor disorder (disorder) |
| 140911000119109 | http://snomed.info/sct | Ischemic stroke with coma (disorder) |
| 14230004 | http://snomed.info/sct | Acquired factor VIII deficiency disease (disorder) |
| 146371000119104 | http://snomed.info/sct | Hepatic coma due to chronic hepatitis C (disorder) |
| 15132005 | http://snomed.info/sct | Acquired factor XII deficiency disease (disorder) |
| 153091000119109 | http://snomed.info/sct | Hepatic coma due to chronic hepatitis B with delta agent (disorder) |
| 154818001 | http://snomed.info/sct | Congenital afibrinogenemia (disorder) |
| 1563006 | http://snomed.info/sct | Protein S deficiency disease (disorder) |
| 15765005 | http://snomed.info/sct | Septic shock due to transfusion (disorder) |
| 16060001 | http://snomed.info/sct | Hepatic coma due to viral hepatitis A (disorder) |
| 16773005 | http://snomed.info/sct | Drug-induced coagulation inhibitor disorder (disorder) |
| 16872008 | http://snomed.info/sct | Severe hereditary factor VIII deficiency disease (disorder) |
| 16922007 | http://snomed.info/sct | Hereditary coagulation factor deficiency (disorder) |
| 1776003 | http://snomed.info/sct | Renal tubular acidosis (disorder) |
| 180481005 | http://snomed.info/sct | Anti-factor II disorder (disorder) |
| 18104000 | http://snomed.info/sct | Metabolic acidosis, normal anion gap, acidifying salts (disorder) |
| 181456001 | http://snomed.info/sct | Antiprothrombin disorder (disorder) |
| 181869007 | http://snomed.info/sct | Neonatal cardiorespiratory arrest (disorder) |
| 183005 | http://snomed.info/sct | Autoimmune pancytopenia (disorder) |
| 18604004 | http://snomed.info/sct | Factor XIII deficiency disease (disorder) |
| 18613002 | http://snomed.info/sct | Miscarriage with septic shock (disorder) |
| 186624004 | http://snomed.info/sct | Hepatic coma due to acute hepatitis B with delta agent (disorder) |
| 186628001 | http://snomed.info/sct | Hepatic coma due to viral hepatitis C (disorder) |
| 190330002 | http://snomed.info/sct | Hyperosmolar coma due to type 1 diabetes mellitus (disorder) |
| 190331003 | http://snomed.info/sct | Hyperosmolar coma due to type 2 diabetes mellitus (disorder) |
| 191296000 | http://snomed.info/sct | Deficiency of coagulation factor due to liver disease (disorder) |
| 191297009 | http://snomed.info/sct | Deficiency of coagulation factor due to vitamin K deficiency (disorder) |
| 191298004 | http://snomed.info/sct | Acquired factor II deficiency (disorder) |
| 191322006 | http://snomed.info/sct | Thrombocytopenia caused by drugs (disorder) |
| 191323001 | http://snomed.info/sct | Thrombocytopenia due to extracorporeal circulation of blood (disorder) |
| 19267009 | http://snomed.info/sct | Lupus anticoagulant disorder (disorder) |
| 19307009 | http://snomed.info/sct | Drug-induced immune thrombocytopenia (disorder) |
| 195506001 | http://snomed.info/sct | Idiopathic hypotension (disorder) |
| 196151000 | http://snomed.info/sct | Pulmonary insufficiency following shock (disorder) |
| 196152007 | http://snomed.info/sct | Pulmonary insufficiency following surgery (disorder) |
| 196153002 | http://snomed.info/sct | Pulmonary insufficiency following trauma (disorder) |
| 200030007 | http://snomed.info/sct | Postpartum coagulation defects - delivered with postnatal problem (disorder) |
| 200031006 | http://snomed.info/sct | Postpartum coagulation defects with postnatal problem (disorder) |
| 200113008 | http://snomed.info/sct | Maternal hypotension syndrome with antenatal problem (disorder) |
| 200114002 | http://snomed.info/sct | Maternal hypotension syndrome with postnatal problem (disorder) |
| 2036003 | http://snomed.info/sct | Acquired factor VII deficiency disease (disorder) |
| 206510008 | http://snomed.info/sct | Transient neonatal thrombocytopenia due to exchange transfusion (disorder) |
| 206511007 | http://snomed.info/sct | Transient neonatal thrombocytopenia due to idiopathic maternal thrombocytopenia (disorder) |
| 206512000 | http://snomed.info/sct | Transient neonatal thrombocytopenia due to isoimmunization (disorder) |
| 21263006 | http://snomed.info/sct | Myxedema coma (disorder) |
| 213215000 | http://snomed.info/sct | Cardiorespiratory failure as a complication of care (disorder) |
| 213258001 | http://snomed.info/sct | Postoperative hypovolemic shock (disorder) |
| 21360006 | http://snomed.info/sct | Miscarriage with afibrinogenemia (disorder) |
| 230499002 | http://snomed.info/sct | Sleep-related respiratory failure (disorder) |
| 230664009 | http://snomed.info/sct | Sympathotonic orthostatic hypotension (disorder) |
| 230795009 | http://snomed.info/sct | Pituitary coma (disorder) |
| 230796005 | http://snomed.info/sct | Non-diabetic hypoglycemic coma (disorder) |
| 230797001 | http://snomed.info/sct | Post-anoxic coma (disorder) |
| 230798006 | http://snomed.info/sct | Hypothermic coma (disorder) |
| 230799003 | http://snomed.info/sct | Post-traumatic coma (disorder) |
| 230800004 | http://snomed.info/sct | Alcoholic coma (disorder) |
| 230801000 | http://snomed.info/sct | Post-ictal coma (disorder) |
| 23205009 | http://snomed.info/sct | Transient neonatal thrombocytopenia (disorder) |
| 233765002 | http://snomed.info/sct | Respiratory failure without hypercapnia (disorder) |
| 234171009 | http://snomed.info/sct | Drug-induced hypotension (disorder) |
| 234173007 | http://snomed.info/sct | Hyperdynamic septic shock (disorder) |
| 234174001 | http://snomed.info/sct | Hypodynamic septic shock (disorder) |
| 234367000 | http://snomed.info/sct | Pancytopenia with pancreatitis (disorder) |
| 234440005 | http://snomed.info/sct | Factor VIII deficiency (disorder) |
| 234442002 | http://snomed.info/sct | Hereditary factor VIII deficiency disease with inhibitor (disorder) |
| 234444001 | http://snomed.info/sct | Congenital factor IX deficiency variant (disorder) |
| 234445000 | http://snomed.info/sct | Congenital factor IX deficiency with inhibitor (disorder) |
| 234451005 | http://snomed.info/sct | Acquired von Willebrand disease (disorder) |
| 234452003 | http://snomed.info/sct | Contact factor deficiency (disorder) |
| 234453008 | http://snomed.info/sct | Passovoy factor deficiency (disorder) |
| 234454002 | http://snomed.info/sct | Prothrombin complex deficiency (disorder) |
| 234455001 | http://snomed.info/sct | Fibrinogen abnormality (disorder) |
| 234456000 | http://snomed.info/sct | Congenital fibrinogen abnormality (disorder) |
| 234457009 | http://snomed.info/sct | Hypofibrinogenemia (disorder) |
| 234458004 | http://snomed.info/sct | Hypodysfibrinogenemia (disorder) |
| 234459007 | http://snomed.info/sct | Alpha chain defect dysfibrinogenemia (disorder) |
| 234460002 | http://snomed.info/sct | Beta chain defect dysfibrinogenemia (disorder) |
| 234461003 | http://snomed.info/sct | Gamma chain defect dysfibrinogenemia (disorder) |
| 234462005 | http://snomed.info/sct | Acquired fibrinogen abnormality (disorder) |
| 234463000 | http://snomed.info/sct | Combined coagulation factor deficiency (disorder) |
| 234464006 | http://snomed.info/sct | Fibrinolytic bleeding syndrome (disorder) |
| 234465007 | http://snomed.info/sct | Alpha-2-antiplasmin deficiency (disorder) |
| 234466008 | http://snomed.info/sct | Acquired coagulation disorder (disorder) |
| 234482009 | http://snomed.info/sct | Amegakaryocytic thrombocytopenia (disorder) |
| 234483004 | http://snomed.info/sct | Megakaryocytic thrombocytopenia (disorder) |
| 234486007 | http://snomed.info/sct | Montreal platelet syndrome (disorder) |
| 234487003 | http://snomed.info/sct | Mediterranean thrombocytopenia (disorder) |
| 236460004 | http://snomed.info/sct | Familial proximal renal tubular acidosis (disorder) |
| 236461000 | http://snomed.info/sct | Distal renal tubular acidosis (disorder) |
| 236463002 | http://snomed.info/sct | Hyperkalemic renal tubular acidosis (disorder) |
| 236464008 | http://snomed.info/sct | Hyporeninemic hypoaldosteronism (disorder) |
| 236467001 | http://snomed.info/sct | Acquired Fanconi syndrome (disorder) |
| 236468006 | http://snomed.info/sct | Adult Fanconi syndrome (disorder) |
| 236541008 | http://snomed.info/sct | Hyperchloremic acidosis associated with dialysis (disorder) |
| 237336007 | http://snomed.info/sct | Fibrinolysis - postpartum (disorder) |
| 237337003 | http://snomed.info/sct | Afibrinogenemia - postpartum (disorder) |
| 237847005 | http://snomed.info/sct | Hyperkalemic acidosis (disorder) |
| 240305000 | http://snomed.info/sct | Neonatal thrombocytopenia due to platelet alloimmunization (disorder) |
| 240464004 | http://snomed.info/sct | Rabies coma (disorder) |
| 24051007 | http://snomed.info/sct | Septic shock following molar AND/OR ectopic pregnancy (disorder) |
| 24149006 | http://snomed.info/sct | Hemorrhagic disease of the newborn due to factor II deficiency (disorder) |
| 24790002 | http://snomed.info/sct | Proximal renal tubular acidosis (disorder) |
| 25904003 | http://snomed.info/sct | Acquired coagulation factor deficiency (disorder) |
| 25966003 | http://snomed.info/sct | Metabolic acidosis caused by methanol (disorder) |
| 25998009 | http://snomed.info/sct | Metabolic acidosis, increased anion gap (disorder) |
| 26029002 | http://snomed.info/sct | Mild hereditary factor VIII deficiency disease (disorder) |
| 26206000 | http://snomed.info/sct | Hepatic coma due to viral hepatitis B (disorder) |
| 26298008 | http://snomed.info/sct | Ketoacidotic coma due to diabetes mellitus (disorder) |
| 267272006 | http://snomed.info/sct | Postpartum coagulation defects (disorder) |
| 267384006 | http://snomed.info/sct | Coma due to hypoglycemia (disorder) |
| 267534000 | http://snomed.info/sct | Primary thrombocytopenia (disorder) |
| 27068000 | http://snomed.info/sct | Failed attempted abortion with afibrinogenemia (disorder) |
| 271870002 | http://snomed.info/sct | Low blood pressure reading (disorder) |
| 27312002 | http://snomed.info/sct | High molecular weight kininogen deficiency (disorder) |
| 273986001 | http://snomed.info/sct | Perinatal thrombocytopenia (disorder) |
| 275470000 | http://snomed.info/sct | Post-cardiorespiratory arrest coma (disorder) |
| 276.2 | http://hl7.org/fhir/sid/icd-9-cm | Acidosis |
| 276259003 | http://snomed.info/sct | Respiratory arrest preceding cardiac arrest (disorder) |
| 276536005 | http://snomed.info/sct | Respiratory insufficiency syndrome of newborn (disorder) |
| 276575001 | http://snomed.info/sct | Autoimmune neonatal thrombocytopenia (disorder) |
| 276586004 | http://snomed.info/sct | Transient neonatal renal tubular acidosis (disorder) |
| 278365007 | http://snomed.info/sct | Anticoagulant-induced bleeding (disorder) |
| 278366008 | http://snomed.info/sct | Anticoagulant excess without bleeding (disorder) |
| 278504009 | http://snomed.info/sct | Afibrinogenemia (disorder) |
| 27942005 | http://snomed.info/sct | Shock (disorder) |
| 281509000 | http://snomed.info/sct | Hypoxic-ischemic coma (disorder) |
| 281510005 | http://snomed.info/sct | Drug-induced coma (disorder) |
| 282707003 | http://snomed.info/sct | Acquired inhibitor of coagulation (disorder) |
| 28293008 | http://snomed.info/sct | Hereditary factor VIII deficiency disease (disorder) |
| 286.6 | http://hl7.org/fhir/sid/icd-9-cm | Defibrination syndrome |
| 286.9 | http://hl7.org/fhir/sid/icd-9-cm | Other and unspecified coagulation defects |
| 28651003 | http://snomed.info/sct | Orthostatic hypotension (disorder) |
| 286963007 | http://snomed.info/sct | Idiopathic chronic hypotension (disorder) |
| 2897005 | http://snomed.info/sct | Immune thrombocytopenia (disorder) |
| 296926001 | http://snomed.info/sct | Heparin overdose (disorder) |
| 296927005 | http://snomed.info/sct | Accidental heparin overdose (disorder) |
| 296928000 | http://snomed.info/sct | Intentional heparin overdose (disorder) |
| 296930003 | http://snomed.info/sct | Coumarin overdose (disorder) |
| 296931004 | http://snomed.info/sct | Accidental coumarin overdose (disorder) |
| 296932006 | http://snomed.info/sct | Intentional coumarin overdose (disorder) |
| 296934007 | http://snomed.info/sct | Accidental warfarin overdose (disorder) |
| 29914000 | http://snomed.info/sct | Dihydrolipoamide dehydrogenase deficiency (disorder) |
| 30182008 | http://snomed.info/sct | Thrombocytopenia due to extracorporeal circulation (disorder) |
| 302215000 | http://snomed.info/sct | Thrombocytopenic disorder (disorder) |
| 302873008 | http://snomed.info/sct | Thrombocytopenic purpura (disorder) |
| 30575002 | http://snomed.info/sct | Fanconi's anemia (disorder) |
| 307342006 | http://snomed.info/sct | Thrombocytopenia due to massive blood transfusion (disorder) |
| 307514008 | http://snomed.info/sct | Idiopathic factor VIII deficiency (disorder) |
| 307515009 | http://snomed.info/sct | Autoimmune factor VIII deficiency (disorder) |
| 307517001 | http://snomed.info/sct | Pregnancy-related factor VIII deficiency (disorder) |
| 307518006 | http://snomed.info/sct | Malignancy-related factor VIII deficiency (disorder) |
| 309775007 | http://snomed.info/sct | Postprocedural respiratory failure (disorder) |
| 31925001 | http://snomed.info/sct | Hereditary factor I deficiency disease (disorder) |
| 323079008 | http://snomed.info/sct | Thrombocytopenia due to sequestration (disorder) |
| 32605001 | http://snomed.info/sct | Transient neonatal disorder of coagulation (disorder) |
| 33169001 | http://snomed.info/sct | Factor XI deficiency, type II (disorder) |
| 33183004 | http://snomed.info/sct | Post infectious thrombocytopenic purpura (disorder) |
| 33297000 | http://snomed.info/sct | Hereditary factor II deficiency disease (disorder) |
| 33344008 | http://snomed.info/sct | Moderate hereditary factor VIII deficiency disease (disorder) |
| 33820001 | http://snomed.info/sct | Acquired factor X deficiency disease (disorder) |
| 34395002 | http://snomed.info/sct | Thrombocytopenia caused by hypothermia (disorder) |
| 34417008 | http://snomed.info/sct | Disseminated intravascular coagulation in newborn (disorder) |
| 34478009 | http://snomed.info/sct | Failed attempted abortion with defibrination syndrome (disorder) |
| 355001 | http://snomed.info/sct | Hemorrhagic shock (disorder) |
| 35528000 | http://snomed.info/sct | Metabolic acidosis caused by salicylate (disorder) |
| 35554008 | http://snomed.info/sct | Acquired factor XI deficiency disease (disorder) |
| 3591006 | http://snomed.info/sct | Metabolic acidosis, normal anion gap, bicarbonate losses (disorder) |
| 359531004 | http://snomed.info/sct | Amegakaryocytic thrombocytopenia with congenital malformation (disorder) |
| 359536009 | http://snomed.info/sct | Megakaryocytic aplasia (disorder) |
| 359700009 | http://snomed.info/sct | Hereditary von Willebrand disease type 1A (disorder) |
| 359711001 | http://snomed.info/sct | Hereditary von Willebrand disease type 2A (disorder) |
| 359717002 | http://snomed.info/sct | Hereditary von Willebrand disease type 2B (disorder) |
| 359723007 | http://snomed.info/sct | Acquired hypofibrinogenemia (disorder) |
| 359725000 | http://snomed.info/sct | Hereditary von Willebrand disease type 2M (disorder) |
| 359727008 | http://snomed.info/sct | Fibrinogen deficiency (disorder) |
| 359730001 | http://snomed.info/sct | Acquired afibrinogenemia (disorder) |
| 359732009 | http://snomed.info/sct | Hereditary von Willebrand disease type 2N (disorder) |
| 36351005 | http://snomed.info/sct | Antithrombin III deficiency (disorder) |
| 370491005 | http://snomed.info/sct | Metabolic acidosis due to grain overload (disorder) |
| 371073003 | http://snomed.info/sct | Postural orthostatic tachycardia syndrome (disorder) |
| 371074009 | http://snomed.info/sct | Radiation thrombocytopenia (disorder) |
| 371106008 | http://snomed.info/sct | Idiopathic maternal thrombocytopenia (disorder) |
| 371632003 | http://snomed.info/sct | Coma (disorder) |
| 371769008 | http://snomed.info/sct | Endotoxic shock (disorder) |
| 37193007 | http://snomed.info/sct | Factor VII deficiency (disorder) |
| 373420004 | http://snomed.info/sct | Upshaw-Schulman syndrome (disorder) |
| 37350004 | http://snomed.info/sct | Hereditary factor X deficiency disease (disorder) |
| 37492005 | http://snomed.info/sct | Sex-linked thrombocytopenia (disorder) |
| 3760002 | http://snomed.info/sct | Familial multiple factor deficiency syndrome, type V (disorder) |
| 38879000 | http://snomed.info/sct | Factor XI inhibitor disorder (disorder) |
| 38970002 | http://snomed.info/sct | Doan-Wright syndrome (disorder) |
| 39191000119103 | http://snomed.info/sct | Disseminated intravascular coagulation due to placental abruption (disorder) |
| 39419009 | http://snomed.info/sct | Hypovolemic shock (disorder) |
| 397767007 | http://snomed.info/sct | Acute respiratory failure requiring reintubation (disorder) |
| 39871006 | http://snomed.info/sct | Chronic respiratory failure (disorder) |
| 39925003 | http://snomed.info/sct | Juvenile myopathy, encephalopathy, lactic acidosis AND stroke (disorder) |
| 402653004 | http://snomed.info/sct | Thrombocytopenic purpura due to defective platelet production (disorder) |
| 402654005 | http://snomed.info/sct | Thrombocytopenic purpura due to platelet consumption (disorder) |
| 402851000 | http://snomed.info/sct | Neonatal purpura fulminans due to homozygous protein C deficiency (disorder) |
| 40855001 | http://snomed.info/sct | Hereditary factor VII deficiency disease (disorder) |
| 408667000 | http://snomed.info/sct | Hemodialysis-associated hypotension (disorder) |
| 408668005 | http://snomed.info/sct | Iatrogenic hypotension (disorder) |
| 40946000 | http://snomed.info/sct | Hepatic coma due to viral hepatitis (disorder) |
| 409622000 | http://snomed.info/sct | Respiratory failure (disorder) |
| 409623005 | http://snomed.info/sct | Respiratory insufficiency (disorder) |
| 410430005 | http://snomed.info/sct | Cardiorespiratory arrest (disorder) |
| 410431009 | http://snomed.info/sct | Cardiorespiratory failure (disorder) |
| 41106001 | http://snomed.info/sct | von Willebrand factor inhibitor disorder (disorder) |
| 41690001 | http://snomed.info/sct | Factor V inhibitor disorder (disorder) |
| 416902009 | http://snomed.info/sct | Uremic thrombocytopenia (disorder) |
| 417626001 | http://snomed.info/sct | Thrombocytopenic purpura associated with metabolic disorder (disorder) |
| 41788008 | http://snomed.info/sct | Hereditary factor IX deficiency disease (disorder) |
| 41816006 | http://snomed.info/sct | Secondary cryofibrinogenemia (disorder) |
| 420270002 | http://snomed.info/sct | Ketoacidosis due to type 1 diabetes mellitus (disorder) |
| 420422005 | http://snomed.info/sct | Ketoacidosis due to diabetes mellitus (disorder) |
| 420662003 | http://snomed.info/sct | Coma due to diabetes mellitus (disorder) |
| 420996007 | http://snomed.info/sct | Coma due to malnutrition-related diabetes mellitus (disorder) |
| 421075007 | http://snomed.info/sct | Ketoacidotic coma due to type 1 diabetes mellitus (disorder) |
| 421437000 | http://snomed.info/sct | Hypoglycemic coma due to type 1 diabetes mellitus (disorder) |
| 421725003 | http://snomed.info/sct | Hypoglycemic coma due to diabetes mellitus (disorder) |
| 421750000 | http://snomed.info/sct | Ketoacidosis due to type 2 diabetes mellitus (disorder) |
| 421766003 | http://snomed.info/sct | Thrombocytopenia with acquired immunodeficiency syndrome (disorder) |
| 421847006 | http://snomed.info/sct | Ketoacidotic coma due to type 2 diabetes mellitus (disorder) |
| 421966007 | http://snomed.info/sct | Non-ketotic non-hyperosmolar coma due to diabetes mellitus (disorder) |
| 422126006 | http://snomed.info/sct | Hyperosmolar coma due to diabetes mellitus (disorder) |
| 422177004 | http://snomed.info/sct | Dyspnea with acquired immunodeficiency syndrome (disorder) |
| 424099008 | http://snomed.info/sct | Hepatic coma due to acute hepatitis B (disorder) |
| 424340000 | http://snomed.info/sct | Hepatic coma due to chronic hepatitis B (disorder) |
| 425949001 | http://snomed.info/sct | Mild hereditary factor VIII deficiency disease with inhibitor (disorder) |
| 426199009 | http://snomed.info/sct | Congenital factor IX deficiency without inhibitor (disorder) |
| 426896000 | http://snomed.info/sct | Chronic hypercapnic respiratory failure (disorder) |
| 427896006 | http://snomed.info/sct | Chronic respiratory insufficiency (disorder) |
| 428173007 | http://snomed.info/sct | Chronic hypoxemic respiratory failure (disorder) |
| 429561008 | http://snomed.info/sct | Exertional hypotension (disorder) |
| 4320005 | http://snomed.info/sct | Factor V deficiency (disorder) |
| 43217004 | http://snomed.info/sct | Hereditary factor XII deficiency disease (disorder) |
| 43253002 | http://snomed.info/sct | Metabolic acidosis caused by ingestion of drugs AND/OR chemicals (disorder) |
| 43302000 | http://snomed.info/sct | Anticoagulant overdosage (disorder) |
| 438360006 | http://snomed.info/sct | Hereditary factor VIII deficiency disease without inhibitor (disorder) |
| 438372000 | http://snomed.info/sct | Hereditary factor IX deficiency disease with inhibitor (disorder) |
| 438373005 | http://snomed.info/sct | Severe hereditary factor VIII deficiency disease with inhibitor (disorder) |
| 438476003 | http://snomed.info/sct | Autoimmune thrombotic thrombocytopenic purpura (disorder) |
| 438599002 | http://snomed.info/sct | Moderate hereditary factor VIII deficiency disease with inhibitor (disorder) |
| 438792009 | http://snomed.info/sct | Hereditary factor IX deficiency disease without inhibitor (disorder) |
| 438827002 | http://snomed.info/sct | Hereditary thrombophilic dysfibrinogenemia (disorder) |
| 439000005 | http://snomed.info/sct | Hyperfibrinogenemia (disorder) |
| 439007008 | http://snomed.info/sct | Acquired thrombotic thrombocytopenic purpura (disorder) |
| 439145006 | http://snomed.info/sct | Congenital hypofibrinogenemia (disorder) |
| 439156006 | http://snomed.info/sct | Acquired combined coagulation factor deficiency (disorder) |
| 439157002 | http://snomed.info/sct | Hereditary combined coagulation factor deficiency (disorder) |
| 439274008 | http://snomed.info/sct | Hereditary protein C deficiency (disorder) |
| 439455002 | http://snomed.info/sct | Hereditary factor XIII A subunit deficiency (disorder) |
| 439458000 | http://snomed.info/sct | Factor I deficiency disease (disorder) |
| 439459008 | http://snomed.info/sct | Hereditary factor XIII B subunit deficiency (disorder) |
| 439460003 | http://snomed.info/sct | Hereditary factor XIII A subunit and B subunit deficiency (disorder) |
| 439699000 | http://snomed.info/sct | Hereditary antithrombin III deficiency (disorder) |
| 439702007 | http://snomed.info/sct | Hereditary protein S deficiency (disorder) |
| 440820004 | http://snomed.info/sct | Mild hereditary factor VIII deficiency disease without inhibitor (disorder) |
| 440866009 | http://snomed.info/sct | Severe hereditary factor IX deficiency disease with inhibitor (disorder) |
| 440867000 | http://snomed.info/sct | Moderate hereditary factor IX deficiency disease with inhibitor (disorder) |
| 440868005 | http://snomed.info/sct | Mild hereditary factor IX deficiency disease with inhibitor (disorder) |
| 440924009 | http://snomed.info/sct | Hereditary hyperfibrinogenemia (disorder) |
| 440988005 | http://snomed.info/sct | Heterozygous protein S deficiency (disorder) |
| 440993008 | http://snomed.info/sct | Severe hereditary factor VIII deficiency disease without inhibitor (disorder) |
| 441006000 | http://snomed.info/sct | Moderate hereditary factor VIII deficiency disease without inhibitor (disorder) |
| 441101007 | http://snomed.info/sct | Heterozygous protein C deficiency (disorder) |
| 441188004 | http://snomed.info/sct | Homozygous protein C deficiency (disorder) |
| 441189007 | http://snomed.info/sct | Homozygous protein S deficiency (disorder) |
| 441190003 | http://snomed.info/sct | Severe hereditary factor IX deficiency disease without inhibitor (disorder) |
| 441191004 | http://snomed.info/sct | Moderate hereditary factor IX deficiency disease without inhibitor (disorder) |
| 441192006 | http://snomed.info/sct | Mild hereditary factor IX deficiency disease without inhibitor (disorder) |
| 441322009 | http://snomed.info/sct | Drug induced thrombotic thrombocytopenic purpura (disorder) |
| 4477007 | http://snomed.info/sct | Juvenile myopathy AND lactate acidosis (disorder) |
| 45007003 | http://snomed.info/sct | Low blood pressure (disorder) |
| 45366001 | http://snomed.info/sct | Hereditary dysfibrinogenemia (disorder) |
| 458.8 | http://hl7.org/fhir/sid/icd-9-cm | Other specified hypotension |
| 458.9 | http://hl7.org/fhir/sid/icd-9-cm | Hypotension, unspecified |
| 45963004 | http://snomed.info/sct | Factor XI deficiency, type III (disorder) |
| 46166004 | http://snomed.info/sct | Compensated metabolic acidosis (disorder) |
| 46683007 | http://snomed.info/sct | Pyruvate dehydrogenase complex deficiency (disorder) |
| 46760003 | http://snomed.info/sct | Estren-Dameshek anemia (disorder) |
| 4690009 | http://snomed.info/sct | Metabolic acidosis caused by paraldehyde (disorder) |
| 46981006 | http://snomed.info/sct | Factor XII deficiency disease (disorder) |
| 47307007 | http://snomed.info/sct | Factor VIII inhibitor disorder (disorder) |
| 47546008 | http://snomed.info/sct | Warfarin overdosage (disorder) |
| 48788004 | http://snomed.info/sct | Cyclic thrombocytopenia (disorder) |
| 48976006 | http://snomed.info/sct | Prekallikrein deficiency (disorder) |
| 49177006 | http://snomed.info/sct | Postpartum coagulation defect with hemorrhage (disorder) |
| 49762007 | http://snomed.info/sct | Hereditary factor XI deficiency disease (disorder) |
| 49886003 | http://snomed.info/sct | Thrombocytopenia due to blood loss (disorder) |
| 50189006 | http://snomed.info/sct | Hereditary factor XIII deficiency disease (disorder) |
| 50770000 | http://snomed.info/sct | Miscarriage with defibrination syndrome (disorder) |
| 51294009 | http://snomed.info/sct | Metabolic acidosis, increased anion gap, accumulation of organic acids (disorder) |
| 51387008 | http://snomed.info/sct | Acidosis (disorder) |
| 51624005 | http://snomed.info/sct | Dilutional thrombocytopenia (disorder) |
| 518.81 | http://hl7.org/fhir/sid/icd-9-cm | Acute respiratory failure |
| 518.82 | http://hl7.org/fhir/sid/icd-9-cm | Other pulmonary insufficiency, not elsewhere classified |
| 55178001 | http://snomed.info/sct | Starvation ketoacidosis (disorder) |
| 55571001 | http://snomed.info/sct | Alcoholic ketoacidosis (disorder) |
| 56051008 | http://snomed.info/sct | Ketoacidosis (disorder) |
| 58067006 | http://snomed.info/sct | Metabolic acidosis, normal anion gap, failure of bicarbonate regeneration (disorder) |
| 58327003 | http://snomed.info/sct | Factor I inhibitor disorder (disorder) |
| 5876000 | http://snomed.info/sct | Acquired pancytopenia (disorder) |
| 58808003 | http://snomed.info/sct | Compensated respiratory acidosis (disorder) |
| 59455009 | http://snomed.info/sct | Metabolic acidosis (disorder) |
| 59686008 | http://snomed.info/sct | Metabolic acidosis caused by ethylene glycol (disorder) |
| 59702004 | http://snomed.info/sct | Compensated acidosis (disorder) |
| 60628003 | http://snomed.info/sct | Mediterranean macrothrombocytopenia (disorder) |
| 609462000 | http://snomed.info/sct | Induced termination of pregnancy complicated by defibrination syndrome (disorder) |
| 61551003 | http://snomed.info/sct | Familial multiple factor deficiency syndrome, type VI (disorder) |
| 61744005 | http://snomed.info/sct | Neonatal thrombocytopenia due to idiopathic maternal thrombocytopenia (disorder) |
| 61802005 | http://snomed.info/sct | Primary cryofibrinogenemia (disorder) |
| 61933008 | http://snomed.info/sct | Hyperadrenergic postural hypotension (disorder) |
| 62698000 | http://snomed.info/sct | Defibrination syndrome following molar AND/OR ectopic pregnancy (disorder) |
| 63444004 | http://snomed.info/sct | Thrombocytopenia due to hypersplenism (disorder) |
| 6364000 | http://snomed.info/sct | Acquired factor XIII deficiency disease (disorder) |
| 64315007 | http://snomed.info/sct | Familial multiple factor deficiency syndrome, type III (disorder) |
| 64509006 | http://snomed.info/sct | Acquired coagulation factor inhibitor disorder (disorder) |
| 64779008 | http://snomed.info/sct | Blood coagulation disorder (disorder) |
| 65710008 | http://snomed.info/sct | Acute respiratory failure (disorder) |
| 65768009 | http://snomed.info/sct | Familial multiple factor deficiency syndrome, type II (disorder) |
| 66909001 | http://snomed.info/sct | Familial multiple factor deficiency syndrome, type IV (disorder) |
| 67406007 | http://snomed.info/sct | Disseminated intravascular coagulation (disorder) |
| 67782005 | http://snomed.info/sct | Acute respiratory distress syndrome (disorder) |
| 67905004 | http://snomed.info/sct | Acute-on-chronic respiratory failure (disorder) |
| 6935003 | http://snomed.info/sct | Familial hemorrhagic diathesis (disorder) |
| 69500007 | http://snomed.info/sct | Blood coagulation disorder due to liver disease (disorder) |
| 698504006 | http://snomed.info/sct | Postoperative cardiopulmonary failure (disorder) |
| 699748007 | http://snomed.info/sct | Cardiorespiratory arrest with successful resuscitation (disorder) |
| 702373006 | http://snomed.info/sct | Hereditary myopathy with early respiratory failure (disorder) |
| 70247006 | http://snomed.info/sct | Hypoadrenergic postural hypotension (disorder) |
| 70644008 | http://snomed.info/sct | Acute respiratory acidosis (disorder) |
| 709109004 | http://snomed.info/sct | Hypercapnic respiratory failure (disorder) |
| 709110009 | http://snomed.info/sct | Acute hypercapnic respiratory failure (disorder) |
| 709111008 | http://snomed.info/sct | Acute hypoxemic respiratory failure (disorder) |
| 70993000 | http://snomed.info/sct | Pyrogenic shock (disorder) |
| 719216001 | http://snomed.info/sct | Hypoglycemic coma due to type 2 diabetes mellitus (disorder) |
| 72836002 | http://snomed.info/sct | Hepatic coma (disorder) |
| 73162004 | http://snomed.info/sct | Posttransfusion purpura (disorder) |
| 73397007 | http://snomed.info/sct | Heparin-induced thrombocytopenia (disorder) |
| 73453007 | http://snomed.info/sct | Irreversible coma (disorder) |
| 73975000 | http://snomed.info/sct | Factor II deficiency (disorder) |
| 74576004 | http://snomed.info/sct | Acquired thrombocytopenia (disorder) |
| 75181005 | http://snomed.info/sct | Chronic orthostatic hypotension (disorder) |
| 75331009 | http://snomed.info/sct | Evans syndrome (disorder) |
| 76407009 | http://snomed.info/sct | Protein C deficiency disease (disorder) |
| 76571007 | http://snomed.info/sct | Septic shock (disorder) |
| 76642003 | http://snomed.info/sct | Factor X deficiency (disorder) |
| 76938004 | http://snomed.info/sct | Infantile encephalopathy AND lactic acidosis (disorder) |
| 77545000 | http://snomed.info/sct | Chronic hypotension (disorder) |
| 776.2 | http://hl7.org/fhir/sid/icd-9-cm | Disseminated intravascular coagulation in newborn |
| 780.01 | http://hl7.org/fhir/sid/icd-9-cm | Coma |
| 78129009 | http://snomed.info/sct | Thrombotic thrombocytopenic purpura (disorder) |
| 78345002 | http://snomed.info/sct | Thrombocytopenia due to diminished platelet production (disorder) |
| 785.50 | http://hl7.org/fhir/sid/icd-9-cm | Shock, unspecified |
| 785.51 | http://hl7.org/fhir/sid/icd-9-cm | Cardiogenic shock |
| 785.52 | http://hl7.org/fhir/sid/icd-9-cm | Septic shock |
| 785.59 | http://hl7.org/fhir/sid/icd-9-cm | Other shock without mention of trauma |
| 786.09 | http://hl7.org/fhir/sid/icd-9-cm | Other respiratory abnormalities |
| 79674009 | http://snomed.info/sct | Hyperheparinemia (disorder) |
| 799.1 | http://hl7.org/fhir/sid/icd-9-cm | Respiratory arrest |
| 80988005 | http://snomed.info/sct | Mixed cryofibrinogenemia (disorder) |
| 81783000 | http://snomed.info/sct | Familial multiple factor deficiency syndrome (disorder) |
| 82190001 | http://snomed.info/sct | Thrombocytopenia due to defective platelet production (disorder) |
| 82835005 | http://snomed.info/sct | Neonatal thrombocytopenia (disorder) |
| 83850008 | http://snomed.info/sct | Acidosis co-occurrent and due to uremia (disorder) |
| 84048006 | http://snomed.info/sct | Familial multiple factor deficiency syndrome, type I (disorder) |
| 85589009 | http://snomed.info/sct | Radial aplasia-thrombocytopenia syndrome (disorder) |
| 85796009 | http://snomed.info/sct | Afibrinogenemia following molar AND/OR ectopic pregnancy (disorder) |
| 86075001 | http://snomed.info/sct | Coagulation factor deficiency syndrome (disorder) |
| 86635005 | http://snomed.info/sct | Kasabach-Merritt syndrome (disorder) |
| 87317003 | http://snomed.info/sct | Respiratory arrest (disorder) |
| 8764008 | http://snomed.info/sct | Chronic respiratory acidosis (disorder) |
| 87902006 | http://snomed.info/sct | Thrombocytopenia due to non-immune destruction (disorder) |
| 88540000 | http://snomed.info/sct | Factor XI deficiency, type I (disorder) |
| 88776002 | http://snomed.info/sct | Hereditary factor V deficiency disease (disorder) |
| 88887003 | http://snomed.info/sct | Maternal hypotension syndrome (disorder) |
| 89138009 | http://snomed.info/sct | Cardiogenic shock (disorder) |
| 89687005 | http://snomed.info/sct | Postimmersion-submersion syndrome (disorder) |
| 89729000 | http://snomed.info/sct | Factor IX inhibitor disorder (disorder) |
| 89962000 | http://snomed.info/sct | Neonatal thrombocytopenia due to exchange transfusion (disorder) |
| 90224001 | http://snomed.info/sct | Coma in the newborn (disorder) |
| 90935002 | http://snomed.info/sct | Hemophilia (disorder) |
| 91273001 | http://snomed.info/sct | Lactic acidosis (disorder) |
| 9489006 | http://snomed.info/sct | Factor X inhibitor disorder (disorder) |
| 95569006 | http://snomed.info/sct | Uremic coma (disorder) |
| 95605009 | http://snomed.info/sct | Hemolysis-elevated liver enzymes-low platelet count syndrome (disorder) |
| 95612000 | http://snomed.info/sct | Neonatal respiratory acidosis (disorder) |
| 95619009 | http://snomed.info/sct | Neonatal respiratory failure (disorder) |
| 95623001 | http://snomed.info/sct | Neonatal coagulation disorder (disorder) |
| 95634003 | http://snomed.info/sct | Neonatal respiratory arrest (disorder) |
| 95839005 | http://snomed.info/sct | Disorder involving the fibrinolytic system (disorder) |
| 95840007 | http://snomed.info/sct | Hypoplasminogenemia (disorder) |
| 95841006 | http://snomed.info/sct | Hereditary hypoplasminogenemia (disorder) |
| 95842004 | http://snomed.info/sct | Autosomal dominant deficiency of plasminogen (disorder) |
| 95843009 | http://snomed.info/sct | Acquired hypoplasminogenemia (disorder) |
| 95844003 | http://snomed.info/sct | Dysplasminogenemia (disorder) |
| 95845002 | http://snomed.info/sct | Hereditary dysplasminogenemia (disorder) |
| 9635004 | http://snomed.info/sct | Late metabolic acidosis of newborn (disorder) |
| D65 | http://hl7.org/fhir/sid/icd-10-cm | Disseminated intravascular coagulation [defibrination syndrome] |
| D68.8 | http://hl7.org/fhir/sid/icd-10-cm | Other specified coagulation defects |
| D68.9 | http://hl7.org/fhir/sid/icd-10-cm | Coagulation defect, unspecified |
| E03.5 | http://hl7.org/fhir/sid/icd-10-cm | Myxedema coma |
| E87.2 | http://hl7.org/fhir/sid/icd-10-cm | Acidosis |
| I95.89 | http://hl7.org/fhir/sid/icd-10-cm | Other hypotension |
| I95.9 | http://hl7.org/fhir/sid/icd-10-cm | Hypotension, unspecified |
| J80 | http://hl7.org/fhir/sid/icd-10-cm | Acute respiratory distress syndrome |
| J96.00 | http://hl7.org/fhir/sid/icd-10-cm | Acute respiratory failure, unspecified whether with hypoxia or hypercapnia |
| J96.01 | http://hl7.org/fhir/sid/icd-10-cm | Acute respiratory failure with hypoxia |
| J96.02 | http://hl7.org/fhir/sid/icd-10-cm | Acute respiratory failure with hypercapnia |
| J96.90 | http://hl7.org/fhir/sid/icd-10-cm | Respiratory failure, unspecified, unspecified whether with hypoxia or hypercapnia |
| J96.91 | http://hl7.org/fhir/sid/icd-10-cm | Respiratory failure, unspecified with hypoxia |
| J96.92 | http://hl7.org/fhir/sid/icd-10-cm | Respiratory failure, unspecified with hypercapnia |
| P60 | http://hl7.org/fhir/sid/icd-10-cm | Disseminated intravascular coagulation of newborn |
| R06.00 | http://hl7.org/fhir/sid/icd-10-cm | Dyspnea, unspecified |
| R06.09 | http://hl7.org/fhir/sid/icd-10-cm | Other forms of dyspnea |
| R06.89 | http://hl7.org/fhir/sid/icd-10-cm | Other abnormalities of breathing |
| R09.2 | http://hl7.org/fhir/sid/icd-10-cm | Respiratory arrest |
| R40.20 | http://hl7.org/fhir/sid/icd-10-cm | Unspecified coma |
| R40.2110 | http://hl7.org/fhir/sid/icd-10-cm | Coma scale, eyes open, never, unspecified time |
| R40.2111 | http://hl7.org/fhir/sid/icd-10-cm | Coma scale, eyes open, never, in the field [EMT or ambulance] |
| R40.2112 | http://hl7.org/fhir/sid/icd-10-cm | Coma scale, eyes open, never, at arrival to emergency department |
| R40.2113 | http://hl7.org/fhir/sid/icd-10-cm | Coma scale, eyes open, never, at hospital admission |
| R40.2114 | http://hl7.org/fhir/sid/icd-10-cm | Coma scale, eyes open, never, 24 hours or more after hospital admission |
| R40.2120 | http://hl7.org/fhir/sid/icd-10-cm | Coma scale, eyes open, to pain, unspecified time |
| R40.2121 | http://hl7.org/fhir/sid/icd-10-cm | Coma scale, eyes open, to pain, in the field [EMT or ambulance] |
| R40.2122 | http://hl7.org/fhir/sid/icd-10-cm | Coma scale, eyes open, to pain, at arrival to emergency department |
| R40.2123 | http://hl7.org/fhir/sid/icd-10-cm | Coma scale, eyes open, to pain, at hospital admission |
| R40.2124 | http://hl7.org/fhir/sid/icd-10-cm | Coma scale, eyes open, to pain, 24 hours or more after hospital admission |
| R40.2210 | http://hl7.org/fhir/sid/icd-10-cm | Coma scale, best verbal response, none, unspecified time |
| R40.2211 | http://hl7.org/fhir/sid/icd-10-cm | Coma scale, best verbal response, none, in the field [EMT or ambulance] |
| R40.2212 | http://hl7.org/fhir/sid/icd-10-cm | Coma scale, best verbal response, none, at arrival to emergency department |
| R40.2213 | http://hl7.org/fhir/sid/icd-10-cm | Coma scale, best verbal response, none, at hospital admission |
| R40.2214 | http://hl7.org/fhir/sid/icd-10-cm | Coma scale, best verbal response, none, 24 hours or more after hospital admission |
| R40.2220 | http://hl7.org/fhir/sid/icd-10-cm | Coma scale, best verbal response, incomprehensible words, unspecified time |
| R40.2221 | http://hl7.org/fhir/sid/icd-10-cm | Coma scale, best verbal response, incomprehensible words, in the field [EMT or ambulance] |
| R40.2222 | http://hl7.org/fhir/sid/icd-10-cm | Coma scale, best verbal response, incomprehensible words, at arrival to emergency department |
| R40.2223 | http://hl7.org/fhir/sid/icd-10-cm | Coma scale, best verbal response, incomprehensible words, at hospital admission |
| R40.2224 | http://hl7.org/fhir/sid/icd-10-cm | Coma scale, best verbal response, incomprehensible words, 24 hours or more after hospital admission |
| R40.2310 | http://hl7.org/fhir/sid/icd-10-cm | Coma scale, best motor response, none, unspecified time |
| R40.2311 | http://hl7.org/fhir/sid/icd-10-cm | Coma scale, best motor response, none, in the field [EMT or ambulance] |
| R40.2312 | http://hl7.org/fhir/sid/icd-10-cm | Coma scale, best motor response, none, at arrival to emergency department |
| R40.2313 | http://hl7.org/fhir/sid/icd-10-cm | Coma scale, best motor response, none, at hospital admission |
| R40.2314 | http://hl7.org/fhir/sid/icd-10-cm | Coma scale, best motor response, none, 24 hours or more after hospital admission |
| R40.2320 | http://hl7.org/fhir/sid/icd-10-cm | Coma scale, best motor response, extension, unspecified time |
| R40.2321 | http://hl7.org/fhir/sid/icd-10-cm | Coma scale, best motor response, extension, in the field [EMT or ambulance] |
| R40.2322 | http://hl7.org/fhir/sid/icd-10-cm | Coma scale, best motor response, extension, at arrival to emergency department |
| R40.2323 | http://hl7.org/fhir/sid/icd-10-cm | Coma scale, best motor response, extension, at hospital admission |
| R40.2324 | http://hl7.org/fhir/sid/icd-10-cm | Coma scale, best motor response, extension, 24 hours or more after hospital admission |
| R40.2340 | http://hl7.org/fhir/sid/icd-10-cm | Coma scale, best motor response, flexion withdrawal, unspecified time |
| R40.2341 | http://hl7.org/fhir/sid/icd-10-cm | Coma scale, best motor response, flexion withdrawal, in the field [EMT or ambulance] |
| R40.2342 | http://hl7.org/fhir/sid/icd-10-cm | Coma scale, best motor response, flexion withdrawal, at arrival to emergency department |
| R40.2343 | http://hl7.org/fhir/sid/icd-10-cm | Coma scale, best motor response, flexion withdrawal, at hospital admission |
| R40.2344 | http://hl7.org/fhir/sid/icd-10-cm | Coma scale, best motor response, flexion withdrawal, 24 hours or more after hospital admission |
| R57.0 | http://hl7.org/fhir/sid/icd-10-cm | Cardiogenic shock |
| R57.1 | http://hl7.org/fhir/sid/icd-10-cm | Hypovolemic shock |
| R57.8 | http://hl7.org/fhir/sid/icd-10-cm | Other shock |
| R57.9 | http://hl7.org/fhir/sid/icd-10-cm | Shock, unspecified |
| R65.21 | http://hl7.org/fhir/sid/icd-10-cm | Severe sepsis with septic shock |
Produced 08 Sep 2023