AOD Thesaurus.  Annotated Hierarchy.  diseases.  GO - GT2.16.4
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GOerespiratory disorder   d-out   qh
NT GU2.4.2e asthma    qh   ah
BT+GK disorder by body system or organ function    qh   ah
+XKe respiratory system    qh   ah
RT EA26e respiration    qh   ah
+EMe respiratory system function    qh   ah
+HG8 respiratory system diagnosis    qh   ah
GO2.  nasal disorder   qh
GO2.2.  .  rhinitis   qh
BT+GO12e respiratory inflammation or infection    qh   ah
GO2.4.  .  sinusitis   qh
BT+GO12e respiratory inflammation or infection    qh   ah
GO4.  apnea   qh
NT GZ28.4e sleep apnea    qh   ah
RT GN4e sudden infant death syndrome    qh   ah
GO6e.  dyspnea   qh
ST respiratory failure
RT+GO16.8 respiratory insufficiency    qh   ah
GO8.  hypoventilation   qh
GO10.  hyperventilation   qh
GO12e.  respiratory inflammation or infection   qh
NT GO2.2 rhinitis    qh   ah
 GO2.4 sinusitis    qh   ah
 GO14.2 bronchitis    qh   ah
+GO16e lung disorder    qh   ah
 GO16.2 pneumonitis    qh   ah
BT+GG16 inflammation or infection    qh   ah
RT+GH16e communicable disease    qh   ah
GO12.2e.  .  pneumonia   qh
RT+GH16e communicable disease    qh   ah
 WH12.6.2 Pneumocystis carinii    qh   ah
GO14e.  bronchial disorder   qh
GO14.2.  .  bronchitis   qh
BT+GO12e respiratory inflammation or infection    qh   ah
GO14.4.  .  bronchospasm   qh
GO16e.  lung disorder   qh
NT GN6.2.2.2 pulmonary hypertension    qh   ah
BT+GO12e respiratory inflammation or infection    qh   ah
RT+GG16.6.2.2e abscess    qh   ah
GO16.2.  .  pneumonitis   qh
BT+GO12e respiratory inflammation or infection    qh   ah
RT+GG16.4e inflammation    qh   ah
GO16.4.  .  pneumoconiosis   qh
BT+GH8e disorder of environmental origin    qh   ah
GO16.6.  .  pulmonary tuberculosis   qh
HN No longer an ETOH descriptor, use *+GH16.14.4.2 tuberculosis* qh ah.
BT+GH16.14.4.2e tuberculosis    qh   ah
GO16.8.  .  respiratory insufficiency   qh
ST respiratory failure
RT GO6e dyspnea    qh   ah
 GZ28.4e sleep apnea    qh   ah
GO16.8.2.  .  .  adult respiratory distress syndrome   qh
GO16.10.  .  chronic obstructive lung disease   qh
GO16.12.  .  pulmonary edema   qh
ST lung edema
BT+GR20.12.2e edema    qh   ah
GO16.14.  .  pulmonary fibrosis   qh
GO16.16e.  .  emphysema   qh
HN ETOH descriptor 2000.
GO16.18.  .  pneumothorax   qh
GO18.  pleural disorder   qh
GO18.2.  .  pleural effusion   qh

GPeoral disorder   d-out   qh
ST mouth disease
BT+GK disorder by body system or organ function    qh   ah
+XL mouth, larynx, vocal organ    qh   ah
RT+ENe oral function    qh   ah
+HG10 mouth, larynx, or vocal organ test    qh   ah
GP8.  oral leukoplakia   qh
GP10.  tongue disorder   qh
GP12e.  dental disorder   qh
RT+GG16.6.2.2e abscess    qh   ah

GQedigestive system disorder   d-out   qh
BT+GK disorder by body system or organ function    qh   ah
+XMe digestive system    qh   ah
RT+EPe digestion    qh   ah
+HG12 digestive system diagnosis    qh   ah
GQ2.  digestive system symptom   qh
BT+GFe symptom    qh   ah
GQ2.2e.  .  dyspepsia   qh
RT GQ6.10.10 gastric dysfunction    qh   ah
GQ2.4e.  .  nausea   qh
HN ETOH descriptor 2000.
GQ2.6e.  .  vomiting   qh
ST emesis
RT GQ2.18.2 hematemesis    qh   ah
 GQ6.10.10 gastric dysfunction    qh   ah
GQ2.8.  .  dysphagia   qh
GQ2.10.  .  diarrhea   qh
RT GQ6.4 infectious gastroenteritis    qh   ah
 GQ6.8.2 intestinal malabsorption    qh   ah
GQ2.12.  .  steatorrhea   qh
RT GQ6.8.2 intestinal malabsorption    qh   ah
GQ2.14.  .  constipation   qh
GQ2.16.  .  abdominal pain   qh
GQ2.18e.  .  gastrointestinal hemorrhage   qh
GQ2.18.2.  .  .  hematemesis   qh
ST vomiting of blood
RT GQ2.6e vomiting    qh   ah
GQ2.18.4.  .  .  bloody stool   qh
ST melena
GQ4e.  esophageal disorder   qh
RT+GG6.2.16e ulcer    qh   ah
+GG6.2.18 perforation    qh   ah
 GG6.6 rupture (body part)    qh   ah
 GH16.16.6 candidiasis    qh   ah
GQ4.2.  .  esophageal diverticula   qh
GQ4.4.  .  esophagitis   qh
RT+GD4 alcohol related disorder    qh   ah
GQ4.8.  .  cardiospasm   qh
GQ4.10.  .  Mallory-Weiss syndrome   qh
ST gastroesophageal laceration-hemorrhage syndrome
RT+GD4 alcohol related disorder    qh   ah
GQ4.12e.  .  esophageal varix   qh
BT+GN10.6.2.2 varicose veins    qh   ah
RT+GD4 alcohol related disorder    qh   ah
 GN6.2.2.4.2e portal hypertension    qh   ah
 GQ10.2.6e alcoholic liver cirrhosis    qh   ah
+GQ10.6.6e liver cirrhosis    qh   ah
 XM2.2.4.8e cardiac junction    qh   ah
GQ4.12.2.  .  .  bleeding esophageal varix   qh
RT GN10.2.2.2e variceal hemorrhage    qh   ah
GQ6e.  gastrointestinal disorder   qh
RT+EP2e gastrointestinal function    qh   ah
+GG6.2.18 perforation    qh   ah
GQ6.2e.  .  peptic ulcer   qh
NT GQ6.10.4e gastric ulcer    qh   ah
BT+GG6.2.16e ulcer    qh   ah
GQ6.4.  .  infectious gastroenteritis   qh
ST gastrointestinal infection
upper intestinal tract inflammation or infection
BT+GH16e communicable disease    qh   ah
RT GH16.14.20 cholera    qh   ah
 GQ2.10 diarrhea    qh   ah
 WE22.8.8 Shigella    qh   ah
GQ6.6e.  .  noninfectious enteritis and colitis   qh
GQ6.6.6.  .  .  inflammatory bowel disease   qh
HN Introduced 2000.
ST IBD
GQ6.6.6.2.  .  .  .  Crohn's disease   qh
GQ6.6.6.4.  .  .  .  colitis   qh
GQ6.6.6.4.2.  .  .  .  .  ulcerative colitis   qh
BT+GG6.2.16e ulcer    qh   ah
GQ6.8.  .  gastrointestinal dysfunction   qh
GQ6.8.2.  .  .  intestinal malabsorption   qh
RT GQ2.10 diarrhea    qh   ah
 GQ2.12 steatorrhea    qh   ah
GQ6.8.4.  .  .  ileus   qh
GQ6.10e.  .  gastric disorder   qh
RT GG6.2.18.2 fistula    qh   ah
GQ6.10.4e.  .  .  gastric ulcer   qh
ST stomach ulcer
BT+GG6.2.16e ulcer    qh   ah
+GQ6.2e peptic ulcer    qh   ah
GQ6.10.6e.  .  .  gastric lesion   qh
GQ6.10.8e.  .  .  gastritis   qh
RT YH2.4.40e gastrin    qh   ah
GQ6.10.8.14e.  .  .  .  alcoholic gastritis   qh
BT+GD4 alcohol related disorder    qh   ah
GQ6.10.10.  .  .  gastric dysfunction   qh
RT GQ2.2e dyspepsia    qh   ah
 GQ2.6e vomiting    qh   ah
GQ6.10.12.  .  .  pyloric dysfunction   qh
RT GG2 motility disorder    qh   ah
GQ6.12e.  .  intestinal disorder   qh
ST bowel disease
BT+XM2e gastrointestinal tract    qh   ah
GQ6.12.4.  .  .  intestinal obstruction   qh
RT+GQ14 hernia of abdominal cavity    qh   ah
GQ6.14.  .  appendicitis   qh
GQ6.16.  .  colonic disorder   qh
RT EP2.14 colon function    qh   ah
GQ6.16.4.  .  .  dysentery   qh
RT WE22.8.8 Shigella    qh   ah
 WH10.2 Entameba histolytica    qh   ah
GQ6.18.  .  anorectal disorder   qh
RT GG6.2.18.2 fistula    qh   ah
GQ8e.  pancreatic disorder   qh
RT EP4e exocrine pancreas function    qh   ah
+GA2.8.6.4 hypofunction    qh   ah
 GA2.8.6.4.2 functional insufficiency    qh   ah
+XM4e pancreas    qh   ah
+XM4.2e exocrine pancreas    qh   ah
GQ8.2e.  .  pancreatitis   qh
GQ8.2.2e.  .  .  acute pancreatitis   qh
GQ8.2.2.2e.  .  .  .  pancreatic abscess   qh
GQ8.2.4e.  .  .  chronic pancreatitis   qh
HN ETOH descriptor 2000.
GQ8.2.6e.  .  .  alcoholic pancreatitis   qh
HN ETOH descriptor 1995.
SN A disorder characterized by inflammation and necrosis of the pancreas, often accompanied by fibrosis and malfunction, related to consumption of hazardous levels of alcohol.
      Alcoholic pancreatitis may be acute or chronic. The acute form presents with upper abdominal pain, anorexia, and vomiting and can be complicated by hypotension, renal failure, lung disease, and psychosis. The chronic form usually presents with recurrent or persistent abdominal pain, anorexia, and weight loss; there may be signs of pancreatic deficiency involving the exocrine functions of the pancreas (e.g., malabsorption, nutritional deficiency) or the endocrine functions (diabetes mellitus).
BT+GD4 alcohol related disorder    qh   ah
GQ8.4e.  .  pancreatic cirrhosis   qh
GQ10e.  liver disorder   qh
ST hepatic disorder
NT+GH16.12.6e viral hepatitis    qh   ah
 GR16.2.2 hepatic porphyria    qh   ah
RT CK10.2e free radicals    qh   ah
+EP6e liver function    qh   ah
 GA2.8.6.4.2 functional insufficiency    qh   ah
 GF2.6.12 abnormal bruising    qh   ah
+GG16.6.2.2e abscess    qh   ah
 GR12.2.4e hemochromatosis    qh   ah
 GR18.2e jaundice    qh   ah
+XM6e liver    qh   ah
GQ10.2e.  .  alcoholic liver disorder   qh
HN ETOH descriptor 1995.
BT+GD4 alcohol related disorder    qh   ah
RT XM6.2.2.4e Mallory's hyalin    qh   ah
GQ10.2.2e.  .  .  alcoholic fatty liver   qh
SN Accumulation of fat in the liver following exposure to hazardous levels of alcohol intake, with consequent enlargement of liver cells and sometimes hepatomegaly, abnormal liver function, nonspecific abdominal pain, anorexia, and less commonly, jaundice. Definitive diagnosis can be made only on histological examination of the liver.
      Fatty liver may develop after only a few days' drinking, and the condition should therefore not be taken to infer a dependence on alcohol. Abstinence results in regression of the histological abnormalities. The preferred term for the condition is "alcohol-induced fatty liver," although it is not in common usage.
      It is not definitely established whether alcoholic fatty liver is a direct precursor of alcoholic hepatitis or cirrhosis.
ST alcohol induced fatty liver
BT+GQ10.6.2e fatty liver    qh   ah
GQ10.2.4e.  .  .  alcoholic hepatitis   qh
HN ETOH descriptor 1995.
SN A disorder of the liver characterized by liver cell necrosis and inflammation following chronic consumption of hazardous levels of alcohol. It is a well-documented precursor of alcoholic cirrhosis, particularly in those whose alcohol intake remains high.
      Although the diagnosis is strictly a histological one, it is often made on the basis of clinical and biochemical evidence, even if confirmation by biopsy is not possible. The diagnosis is suggested on clinical grounds by the presence of jaundice (which may be deep) and tender hepatomegaly, sometimes with ascites and hemorrhage.
RT+GG14.6e necrosis    qh   ah
GQ10.2.4.2e.  .  .  .  acute alcoholic hepatitis   qh
BT+GD4 alcohol related disorder    qh   ah
+GQ10.6.4e noninfectious hepatitis    qh   ah
GQ10.2.6e.  .  .  alcoholic liver cirrhosis   qh
SN A severe form of alcoholic liver disease, characterized by necrosis and permanent architectural distortion of the liver due to fibrous tissue formation and regeneratory nodules. This is a strictly histological definition, but diagnosis is often made on clinical grounds only.
      Alcoholic liver cirrhosis occurs mainly in the 40-60 year age group, after at least 10 years of hazardous drinking. Individuals show symptoms and signs of hepatic decompensation such as ascites, ankle edema, jaundice, bruising, gastrointestinal hemorrhage from esophageal varices, and confusion or stupor due to hepatic encephalopathy. About 30 percent of patients are "well compensated" at the time of diagnosis and present with nonspecific complaints such as abdominal pain, bowel disturbance, weight loss, and muscle wasting and weakness. Liver cancer is a late complication of cirrhosis in approximately 15 percent of cases.
ST alcoholic cirrhosis
BT+GD4 alcohol related disorder    qh   ah
+GQ10.6.6e liver cirrhosis    qh   ah
+GQ10.6.8e portal cirrhosis    qh   ah
RT+GG14.6e necrosis    qh   ah
+GQ4.12e esophageal varix    qh   ah
 GQ16.2e ascites    qh   ah
 GR18.2e jaundice    qh   ah
 GT2.6.20.4 spur cell anemia    qh   ah
 GX4.16.2.4e hepatic encephalopathy    qh   ah
GQ10.4e.  .  liver abscess   qh
BT+GG16.6.2.2e abscess    qh   ah
GQ10.6e.  .  chronic liver disease   qh
RT GN6.2.2.4.2e portal hypertension    qh   ah
 GR12.4.2 Wilson's disease    qh   ah
 GS2.2.4 hepatorenal syndrome    qh   ah
 GX4.16.2.4e hepatic encephalopathy    qh   ah
GQ10.6.2e.  .  .  fatty liver   qh
ST hepatic steatosis
NT GQ10.2.2e alcoholic fatty liver    qh   ah
GQ10.6.4e.  .  .  noninfectious hepatitis   qh
NT GQ10.2.4.2e acute alcoholic hepatitis    qh   ah
GQ10.6.6e.  .  .  liver cirrhosis   qh
SN A disease characterized by fibrosis, nodules, and loss of the normal structure of the liver accompanied by decline in liver function.
ST cirrhosis
hepatic cirrhosis
liver scarring
NT GQ10.2.6e alcoholic liver cirrhosis    qh   ah
RT+GQ4.12e esophageal varix    qh   ah
GQ10.6.6.2e.  .  .  .  biliary liver cirrhosis   qh
HN ETOH descriptor 2000.
ST cholangitic cirrhosis
cholestatic cirrhosis
GQ10.6.8e.  .  .  portal cirrhosis   qh
ST Laennec's cirrhosis
NT GQ10.2.6e alcoholic liver cirrhosis    qh   ah
GQ10.8e.  .  hepatomegaly   qh
HN ETOH descriptor 2000.
ST hepatic enlargement
BT+GG8 distortion or displacement of body part    qh   ah
GQ12e.  biliary and gallbladder disorder   qh
RT GA2.8.6.4.2 functional insufficiency    qh   ah
+XM8e gallbladder    qh   ah
+XM10e biliary tract    qh   ah
GQ12.2e.  .  cholestasis   qh
HN ETOH descriptor 1995.
RT GR18.2e jaundice    qh   ah
GQ12.4e.  .  cholelithiasis   qh
HN ETOH descriptor 1995.
RT EB26e bile acid metabolism    qh   ah
GQ12.4.2.  .  .  choledocholithiasis   qh
GQ12.4.4e.  .  .  gallstone   qh
HN ETOH descriptor 1995.
ST calculus of gallbladder
GQ12.8.  .  biliary obstruction   qh
ST bile duct obstruction
biliary stenosis or stricture
GQ12.10.  .  cholecystitis   qh
ST acute cholecystitis
GQ14.  hernia of abdominal cavity   qh
RT GQ6.12.4 intestinal obstruction    qh   ah
GQ14.4.  .  diaphragmatic hernia   qh
ST paraesophageal hernia
GQ14.4.4.  .  .  hiatal hernia   qh
GQ16e.  peritoneal disorder   qh
GQ16.2e.  .  ascites   qh
BT+GG12.2 abnormal secretion    qh   ah
RT GQ10.2.6e alcoholic liver cirrhosis    qh   ah
GQ16.4e.  .  peritonitis   qh
BT+GG16.4e inflammation    qh   ah
+GH16e communicable disease    qh   ah

GRemetabolic disorder   d-out   qh
NT GL6.2 muscular dystrophy    qh   ah
BT+GK disorder by body system or organ function    qh   ah
RT+EBe metabolism    qh   ah
+GH14e nutritional disorder    qh   ah
+GJ2e intrauterine disorder    qh   ah
+GVe endocrine disorder    qh   ah
GR2e.  ethanol metabolism disorder   qh
ST disorders of ethanol metabolism
BT+BB2e ethanol    qh   ah
+GD4 alcohol related disorder    qh   ah
+GR4e carbohydrate metabolism disorder    qh   ah
RT+EB10.12e ethanol metabolism    qh   ah
+YC14.2.2e alcohol dehydrogenases    qh   ah
+YC14.4.2e aldehyde dehydrogenases    qh   ah
GR2.2e.  .  alcohol flush reaction   qh
SN Flushing of the face, neck, and shoulders after the ingestion of alcohol, often accompanied by nausea, dizziness, and palpitations. The alcohol flush reaction is seen in approximately 50 percent of Asian (Mongoloid) racial groups. It is caused by an inherited deficiency of the enzyme aldehyde dehydrogenase, which catalyzes the breakdown of acetaldehyde. The reaction also occurs when alcohol is taken by a person receiving treatment with alcohol sensitizing drugs such as disulfiram, which inhibit aldehyde dehydrogenase.
ST alcohol flushing reaction
BT+GF2.6.8 flushing    qh   ah
RT+GD4 alcohol related disorder    qh   ah
 HB4.6.2.8.4 alcohol-related genetic markers    qh   ah
+TH8.4e Asian    qh   ah
+XH2e skin    qh   ah
+YC14.4.2e aldehyde dehydrogenases    qh   ah
+YD8.2 ADH antagonists    qh   ah
+ZG2.4e acetaldehyde    qh   ah
GR4e.  carbohydrate metabolism disorder   qh
ST disorders of carbohydrate metabolism
disorders of carbohydrate metabolism and transport
NT+GR2e ethanol metabolism disorder    qh   ah
BT+ZHe carbohydrates    qh   ah
RT+EB12e carbohydrate metabolism    qh   ah
 GV12.2.2 diabetes mellitus    qh   ah
GR4.10e.  .  glucose intolerance   qh
HN Introduced 2000.
GR4.12e.  .  hyperglycemia   qh
RT+ZH2.12.2e glucose    qh   ah
GR4.14e.  .  hypoglycemia   qh
RT+ZH2.12.2e glucose    qh   ah
 ZM8e phenformin    qh   ah
GR4.16e.  .  hyperinsulinemia   qh
HN Introduced 2000.
GR6e.  lipid metabolism disorder   qh
ST disorders of lipid metabolism
BT+ZK2e lipids    qh   ah
RT EB14e lipid metabolism    qh   ah
GR6.10e.  .  hyperlipidemia   qh
GR6.12e.  .  hypercholesterolemia   qh
ST high blood cholesterol level
RT HF18.2 cholesterol level    qh   ah
GR8e.  amino acid metabolism disorder   qh
ST disorders of amino acid metabolism
BT+ZO2e amino acids    qh   ah
RT+EB16e amino acid metabolism    qh   ah
GR10e.  protein metabolism disorder   qh
BT+ZO6e proteins    qh   ah
RT EB18e protein metabolism    qh   ah
GR10.2.  .  hypoproteinemia   qh
RT+ZO6.4.10e blood proteins    qh   ah
GR10.4.  .  hemoglobinopathies   qh
RT+GT2.6e anemia    qh   ah
+GT2.6.12 hemoglobinopathic anemia    qh   ah
 GT2.6.12.2 sickle cell anemia    qh   ah
GR10.6.  .  plasma protein disorder   qh
ST disorders of plasma protein metabolism
GR10.6.8.  .  .  hyperlipoproteinemia   qh
GR12e.  mineral metabolism disorder   qh
ST disorders of mineral metabolism
BT+YA4e mineral nutrients    qh   ah
RT+EB28e mineral metabolism    qh   ah
GR12.2e.  .  iron metabolism disorder   qh
ST disorders of iron metabolism
BT+ZA2.20.2.10e iron    qh   ah
RT EB28.6e iron metabolism    qh   ah
GR12.2.4e.  .  .  hemochromatosis   qh
HN ETOH descriptor 1995.
RT+GQ10e liver disorder    qh   ah
+ZA2.20.2.10e iron    qh   ah
GR12.2.6.  .  .  hemosiderosis   qh
GR12.4.  .  copper metabolism disorder   qh
ST disorders of copper metabolism
BT+ZA2.20.2.16e copper    qh   ah
GR12.4.2.  .  .  Wilson's disease   qh
ST hepatolenticular degeneration
RT+GQ10.6e chronic liver disease    qh   ah
GR12.6e.  .  magnesium metabolism disorder   qh
ST disorders of magnesium metabolism
NT GR20.20 hypomagnesemia    qh   ah
BT+ZA2.4.4.4e magnesium    qh   ah
RT+GR20e disorder of fluid or electrolyte or acid-base balance    qh   ah
GR12.8.  .  phosphorus metabolism disorder   qh
ST disorders of phosphorus metabolism
BT+ZA2.12.4e phosphorus    qh   ah
RT EB28.4e phosphorus metabolism    qh   ah
GR12.10e.  .  calcium metabolism disorder   qh
ST disorders of calcium metabolism
BT+ZA2.4.4.6e calcium    qh   ah
RT EB28.2.2 calcification    qh   ah
 EB28.2.4 decalcification    qh   ah
GR12.10.6.  .  .  hypercalcemia   qh
GR12.10.8.  .  .  hypercalciuria   qh
GR14.  cystic fibrosis   qh
ST fibrocystic disease of the pancreas
mucoviscidosis
GR16.  porphyrin disorder   qh
ST disorders of porphyrin metabolism
BT+ZT4.30.2e porphyrins    qh   ah
GR16.2.  .  porphyria   qh
RT+GD4 alcohol related disorder    qh   ah
GR16.2.2.  .  .  hepatic porphyria   qh
BT+GQ10e liver disorder    qh   ah
GR18.  hyperbilirubinemia   qh
RT+ZT4.30.4e bilirubin    qh   ah
GR18.2e.  .  jaundice   qh
BT+GF2.6 cutaneous symptom    qh   ah
RT+GQ10e liver disorder    qh   ah
 GQ10.2.6e alcoholic liver cirrhosis    qh   ah
 GQ12.2e cholestasis    qh   ah
+GT2.6.20e hemolytic anemia    qh   ah
GR20e.  disorder of fluid or electrolyte or acid-base balance   qh
BT+YM4e biological electrolytes    qh   ah
RT+EB2e homeostasis    qh   ah
+GR12.6e magnesium metabolism disorder    qh   ah
GR20.4.  .  hyperosmolality   qh
GR20.4.2.  .  .  hypernatremia   qh
ST sodium excess
RT CF14.6.2e osmolality    qh   ah
GR20.6.  .  hypo-osmolality   qh
RT CF14.6.2e osmolality    qh   ah
GR20.6.2e.  .  .  hyponatremia   qh
HN ETOH descriptor 2000.
GR20.8.  .  acid-base imbalance   qh
GR20.8.2e.  .  .  acidosis   qh
HN ETOH descriptor 1995.
GR20.8.2.6e.  .  .  .  lactic acidosis   qh
HN Changed descriptor 2000; through 1999 use "lactacidosis." ETOH descriptor 2000.
ST lactacidosis
GR20.8.2.8e.  .  .  .  ketoacidosis   qh
HN ETOH descriptor 1995.
GR20.8.2.8.2e.  .  .  .  .  alcoholic ketoacidosis   qh
HN Introduced 2000.
BT+GD4 alcohol related disorder    qh   ah
GR20.8.4e.  .  .  alkalosis   qh
HN ETOH descriptor 2000.
GR20.10.  .  dehydration   qh
ST hypovolemia
volume depletion
RT GN6.4.2.4 hypovolemic shock    qh   ah
GR20.12.  .  fluid overload   qh
ST fluid retention
RT EE12.6.8e drug retention    qh   ah
GR20.12.2e.  .  .  edema   qh
HN ETOH descriptor 1995.
NT GO16.12 pulmonary edema    qh   ah
BT+GG12.2 abnormal secretion    qh   ah
RT+EA8e biological regulation    qh   ah
GR20.20.  .  hypomagnesemia   qh
ST low blood magnesium level
BT+GR12.6e magnesium metabolism disorder    qh   ah
GR22.  gout   qh
GR24.  amyloidosis   qh

GSeurogenital disorder   d-out   qh
ST genitourinary disorder
BT+GK disorder by body system or organ function    qh   ah
GS2e.  urinary system disorder   qh
ST urologic disease
BT+XPe urinary system    qh   ah
RT+ERe urinary system function    qh   ah
+HG14 urologic diagnosis    qh   ah
GS2.2e.  .  kidney disorder   qh
ST nephrologic disease
nephropathy
renal disease
NT GN6.2.6.4 renal hypertension    qh   ah
GS2.2.2e.  .  .  nephrotic syndrome   qh
HN Introduced 2000.
ST nephrosis
GS2.2.4.  .  .  hepatorenal syndrome   qh
RT+GQ10.6e chronic liver disease    qh   ah
GS2.2.6.  .  .  nephrolithiasis   qh
ST kidney stones
GS2.2.8.  .  .  kidney failure   qh
ST renal failure
GS4.  reproductive system disorder   qh
BT+XQe reproductive system    qh   ah
RT+HG16e reproductive system diagnosis    qh   ah
GS4.2e.  .  genital disorder   qh
RT+ESe reproductive function    qh   ah
+GH16.8.4e sexually transmitted disease    qh   ah
+GZ30e psychosexual disorder    qh   ah
GS4.2.2.  .  .  organic sexual dysfunction   qh
ST sexual dysfunction
GS4.2.2.2.  .  .  .  organic impotence   qh
RT+GZ30.4e psychosexual dysfunction    qh   ah
GS4.2.2.4e.  .  .  .  infertility   qh
HN ETOH descriptor 2000.
ST sterility
BT+ES2e fertility    qh   ah
RT+PB6.10 fertility rate    qh   ah
GS4.2.4e.  .  .  feminization   qh
SN The development in the male of secondary sex characters of a female.
RT+GVe endocrine disorder    qh   ah
GS4.2.6.  .  .  testicular atrophy   qh
RT+ES4e gonad function    qh   ah
+ES4.6e testicular function    qh   ah
GS4.2.8.  .  .  hypogonadism   qh

GTeblood system disorder   d-out   qh
ST hematolymphatic disease
BT+GK disorder by body system or organ function    qh   ah
+XSe blood    qh   ah
GT2e.  blood disorder   qh
BT+XSe blood    qh   ah
RT+ET2e blood function    qh   ah
+HF16e hematologic test    qh   ah
+HF18e blood chemistry    qh   ah
 HQ6.6 hemodilution    qh   ah
GT2.2e.  .  bone marrow disorder   qh
GT2.4.  .  pancytopenia   qh
RT+XS2e blood cells    qh   ah
GT2.6e.  .  anemia   qh
RT EB28.6e iron metabolism    qh   ah
 ET2.8.2 erythropoiesis    qh   ah
 GF2.14 hypoxemia    qh   ah
+GN10.2.2e hemorrhage    qh   ah
 GR10.4 hemoglobinopathies    qh   ah
 XS2.6e erythrocytes    qh   ah
+ZO6.4.10.2e hemoglobin    qh   ah
GT2.6.10.  .  .  aplastic anemia   qh
ST aregenerative anemia
GT2.6.12.  .  .  hemoglobinopathic anemia   qh
BT+GT2.16.4 congenital hemolytic anemia    qh   ah
RT GR10.4 hemoglobinopathies    qh   ah
GT2.6.12.2.  .  .  .  sickle cell anemia   qh
ST drepanocytosis
Herrick's anemia
meniscocytic anemia
microdrepanocytic anemia
BT+GT2.6.20e hemolytic anemia    qh   ah
RT GR10.4 hemoglobinopathies    qh   ah
GT2.6.12.4.  .  .  .  thalassemia   qh
GT2.6.14e.  .  .  macrocytic anemia   qh
HN ETOH descriptor 2000.
ST megalocytic anemia
GT2.6.14.2.  .  .  .  folic acid deficiency anemia   qh
BT+YB12.6e folic acid    qh   ah
GT2.6.14.2.2e.  .  .  .  .  macrocytosis   qh
HN ETOH descriptor 1995.
ST macrocythemia
megalocythemia
megalocytosis
GT2.6.14.2.4e.  .  .  .  .  megaloblastic anemia   qh
HN ETOH descriptor 2000.
RT+YB12.6e folic acid    qh   ah
 ZO6.8.12.10.4e intrinsic factor    qh   ah
GT2.6.14.2.4.2.  .  .  .  .  .  pernicious anemia   qh
ST Addison's anemia
Biermer's anemia
malignant anemia
RT+YB12.24e vitamin B12    qh   ah
GT2.6.16.  .  .  hyperchromic anemia   qh
HN Introduced 2000.
GT2.6.16.2e.  .  .  .  iron deficiency anemia   qh
HN ETOH descriptor 2000.
ST ferropenic anemia
hypoferric anemia
sideropenic anemia
GT2.6.16.2.2.  .  .  .  .  iron loading anemia   qh
GT2.6.18.  .  .  sideroblastic anemia   qh
RT+BBe alcohol in any form    qh   ah
 YB12.18e pyridoxine    qh   ah
+ZA2.4.4.4e magnesium    qh   ah
 ZA2.10.10e lead    qh   ah
GT2.6.20e.  .  .  hemolytic anemia   qh
HN ETOH descriptor 2000.
ST glucose-6-phosphate dehydrogenase deficiency
icterohemolytic anemia
toxic hemolytic anemia
NT GT2.6.12.2 sickle cell anemia    qh   ah
RT ET2.10e hemolysis    qh   ah
 GR18.2e jaundice    qh   ah
GT2.6.20.2.  .  .  .  immunohemolytic anemia   qh
ST autoimmune hemolytic anemia
immune complex hemolytic anemia
RT GT2.8 blood group incompatibility    qh   ah
GT2.6.20.4.  .  .  .  spur cell anemia   qh
ST acanthocytosis
RT GQ10.2.6e alcoholic liver cirrhosis    qh   ah
GT2.8.  .  blood group incompatibility   qh
BT+GUe immune disorder    qh   ah
RT GT2.6.20.2 immunohemolytic anemia    qh   ah
 XS2.6e erythrocytes    qh   ah
GT2.10.  .  leukocyte disorder   qh
NT+GT2.12.4 platelet disorder    qh   ah
GT2.12.  .  blood coagulation disorder   qh
ST coagulopathy
RT+ET2.4e blood coagulation    qh   ah
 YB18e vitamin K    qh   ah
GT2.12.2.  .  .  hereditary coagulopathy   qh
GT2.12.4.  .  .  platelet disorder   qh
ST thrombocyte disorders
BT+GT2.10 leukocyte disorder    qh   ah
GT2.12.4.4e.  .  .  .  thrombocytopenia   qh
HN ETOH descriptor 1995.
GT2.12.4.6.  .  .  .  platelet dysfunction   qh
RT ET2.4.2.2e platelet aggregation    qh   ah
GT2.12.6.  .  .  vascular purpura   qh
GT2.14e.  .  thrombosis   qh
HN ETOH descriptor 1995.
SN The formation of a blood clot.
RT+GN6.10e vascular ischemia    qh   ah
+GN10e vascular disorder    qh   ah
 GN10.8.2.2 thrombophlebitis    qh   ah
GT2.16.  .  congenital blood disorder   qh
RT+GJ4.2e congenital anomaly    qh   ah
GT2.16.2.  .  .  congenital plasma protein disorder   qh
GT2.16.4.  .  .  congenital hemolytic anemia   qh
NT+GT2.6.12 hemoglobinopathic anemia    qh   ah


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