AOD Thesaurus.  Annotated Hierarchy.  diseases.  GU - GY14
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GUeimmune disorder   d-out   qh
NT GT2.8 blood group incompatibility    qh   ah
BT+GK disorder by body system or organ function    qh   ah
+XTe immune system    qh   ah
RT+ET4e immune function    qh   ah
+HF20e immunologic test    qh   ah
GU2.  immediate hypersensitivity   qh
SN A condition in which components of the immune system overreact or respond in an inappropriate manner, causing tissue damage.
ST type I immunologic disease
RT+EE14.4.4.4.2e toxic drug effect    qh   ah
 ET4.2.4.2.2 IgE-mediated immediate hypersensitivity    qh   ah
GU2.2.  .  anaphylaxis   qh
GU2.4.  .  atopy   qh
ST allergy
atopic hypersensitivity
NT GM4.4 atopic dermatitis    qh   ah
GU2.4.2e.  .  .  asthma   qh
HN ETOH descriptor 2000.
BT+GOe respiratory disorder    qh   ah
GU2.4.4.  .  .  hay fever   qh
GU2.6.  .  skin hypersensitivity   qh
NT GM4.4 atopic dermatitis    qh   ah
 GM4.6 contact dermatitis    qh   ah
 GM4.8e eczema    qh   ah
RT+GMe skin disorder    qh   ah
GU4e.  immunodeficiency   qh
RT ET4.4.4e immunosuppressive effect    qh   ah
 GH16.12.20.2.2e acquired immunodeficiency syndrome    qh   ah
GU6e.  autoimmune disorder   qh
NT GL10.6.2 rheumatoid arthritis    qh   ah
 GL16.8 systemic lupus erythematosus    qh   ah
 GX2.4 myasthenia gravis    qh   ah
GU6.2.  .  lymphatic disorder   qh
GU6.4.  .  spleen disorder   qh
GU6.6.  .  thymus disorder   qh

GVeendocrine disorder   d-out   qh
NT+GN6.2.6 endocrinal hypertension    qh   ah
BT+GK disorder by body system or organ function    qh   ah
+XUe endocrine system    qh   ah
RT EB22e hormone metabolism    qh   ah
+EUe endocrine function    qh   ah
+GRe metabolic disorder    qh   ah
 GS4.2.4e feminization    qh   ah
+HG18e endocrine diagnosis    qh   ah
GV4e.  hypothalamic disorder   qh
RT GZ24.8e anorexia nervosa    qh   ah
GV6e.  pituitary disorder   qh
GV6.2.  .  pituitary hyperfunction   qh
ST hyperpituitarism
BT+GA2.8.6.2 hyperfunction    qh   ah
GV6.4.  .  pituitary hypofunction   qh
ST hypopituitarism
pituitary dwarfism
GV6.4.2.  .  .  Cushing's disease   qh
RT GV14.2.8.2 Cushing's syndrome    qh   ah
GV8e.  thyroid disorder   qh
GV8.4.  .  goiter   qh
GV8.6.  .  hyperthyroidism   qh
GV8.6.4.  .  .  Grave's disease   qh
GV8.6.6.  .  .  thyrotoxicosis   qh
ST thyroid storm
GV8.8.  .  hypothyroidism   qh
ST cretinism
myxedema
GV10e.  parathyroid disorder   qh
GV10.2.  .  hyperparathyroidism   qh
GV10.4.  .  hypoparathyroidism   qh
GV12.  endocrine pancreas disorder   qh
ST pancreatic islet disorders
GV12.2e.  .  diabetes   qh
SN Index here nonspecific diabetes or specific types other than diabetes mellitus.
GV12.2.2.  .  .  diabetes mellitus   qh
RT+GR4e carbohydrate metabolism disorder    qh   ah
GV14e.  adrenal disorder   qh
GV14.2.  .  adrenal cortical disorder   qh
GV14.2.4.  .  .  adrenal cortical hyperfunction   qh
BT+GA2.8.6.2 hyperfunction    qh   ah
GV14.2.4.2.  .  .  .  hyperaldosteronism   qh
GV14.2.6.  .  .  adrenal cortical hypofunction   qh
GV14.2.6.2.  .  .  .  Addison's disease   qh
GV14.2.6.4.  .  .  .  hypoaldosteronism   qh
GV14.2.8.  .  .  adrenal cortical insufficiency   qh
GV14.2.8.2.  .  .  .  Cushing's syndrome   qh
SN Do not confuse with *GV6.4.2 Cushing's disease* qh ah.
GV14.4.  .  adrenal medulla disorder   qh

GWesensory system disorder   d-out   qh
ST sensory function defect
BT+GK disorder by body system or organ function    qh   ah
+XVe sensory system    qh   ah
RT+EVe sensory system function    qh   ah
+FGe sensory perception    qh   ah
+GF2.24e sensory disturbance    qh   ah
+GJ2.16.2.4e alcohol-related intrauterine disorder    qh   ah
+GZ2.4 perceptual disturbance    qh   ah
+HG20e sensory system diagnosis    qh   ah
GW2.  sense organ disorder   qh
NT+GW8.2 eye disorder    qh   ah
 GW10.2 ear disorder    qh   ah
BT+XV2 sense organ    qh   ah
RT+FH cognition, learning, and memory    qh   ah
GW4e.  sensory nerve disorder   qh
SN This includes disorders of sensory nerves or sensory processing in the brain.
NT+GW8.4e vision disorder    qh   ah
+GW10.4 hearing disorder    qh   ah
BT+GK disorder by body system or organ function    qh   ah
+XV4e sensory nervous system    qh   ah
RT+EV2e sensation    qh   ah
+GW12e olfactory system disorder    qh   ah
+XV4.2e sensory receptors    qh   ah
GW4.2.  .  peripheral and central sensory disorder   qh
GW4.2.2e.  .  .  peripheral sensory disorder   qh
RT+GF2.24.2 dysesthesia    qh   ah
GW4.2.4e.  .  .  central sensory disorder   qh
RT+GF2.24.2 dysesthesia    qh   ah
+XV6.6.4.2e optic nerve    qh   ah
+XZ2.6e CNS nuclei    qh   ah
GW6e.  sensory motor system disorder   qh
RT+EV2e sensation    qh   ah
 EW14 sensorimotor integration    qh   ah
+XV4.2e sensory receptors    qh   ah
 XY6.2 somatic nervous system    qh   ah
+XY6.4e autonomic nervous system    qh   ah
GW8e.  visual system disorder   qh
BT+XV6 visual system    qh   ah
RT+FG28e visual perception    qh   ah
 GF2.24.4e vision disturbance    qh   ah
GW8.2.  .  eye disorder   qh
ST oculopathy
NT+GW8.4e vision disorder    qh   ah
BT+GW2 sense organ disorder    qh   ah
+XV6.2e eye    qh   ah
GW8.2.10.  .  .  glaucoma   qh
RT+GG10.6 interrupted transit or circulation    qh   ah
GW8.2.12.  .  .  conjunctivitis   qh
RT+GG16.4e inflammation    qh   ah
+GH16e communicable disease    qh   ah
GW8.2.14.  .  .  corneal disorder   qh
GW8.2.16.  .  .  lens disorder   qh
BT+XV6.2.4.14 lens (eye)    qh   ah
GW8.2.16.2.  .  .  .  cataract   qh
GW8.2.18.  .  .  retinal disorder   qh
ST retinopathy
BT+XV6.2.4.16e retina    qh   ah
GW8.2.20.  .  .  eye refraction disorder   qh
BT+GW8.4.2e impaired visual acuity    qh   ah
GW8.2.22.  .  .  eyelid disorder   qh
BT+XV6.2.6 eyelid    qh   ah
GW8.4e.  .  vision disorder   qh
HN ETOH descriptor 2000.
ST visual defect
BT+GW4e sensory nerve disorder    qh   ah
+GW8.2 eye disorder    qh   ah
+XV6.6 visual nerve system    qh   ah
RT+EV4.4e vision    qh   ah
 GF2.24.4e vision disturbance    qh   ah
+GY8e language or speech disorder    qh   ah
GW8.4.2e.  .  .  impaired visual acuity   qh
HN Introduced 2000.
NT GW8.2.20 eye refraction disorder    qh   ah
BT+FG28.6 visual acuity    qh   ah
+GA2.8e impaired health    qh   ah
GW8.4.4.  .  .  blindness   qh
ST amaurosis
GW8.4.6.  .  .  amblyopia   qh
RT XV6.6.6e visual cortex    qh   ah
GW8.4.6.2.  .  .  .  toxic amblyopia   qh
GW8.4.6.4.  .  .  .  color blindness   qh
ST color amblyopia
RT EV4.4.8 color vision    qh   ah
 HB4.6.2.8.4 alcohol-related genetic markers    qh   ah
GW8.4.8.  .  .  scotoma   qh
GW8.4.8.2.  .  .  .  hemianopia   qh
GW8.4.10.  .  .  night blindness   qh
ST nyctalopia
GW10e.  auditory system disorder   qh
ST auditory defect
BT+XV8 auditory system    qh   ah
RT+FG30e auditory perception    qh   ah
 GF2.24.6 auditory disturbance    qh   ah
GW10.2.  .  ear disorder   qh
BT+GW2 sense organ disorder    qh   ah
+XV8.2e ear    qh   ah
GW10.4.  .  hearing disorder   qh
ST hearing impairment
BT+GW4e sensory nerve disorder    qh   ah
+XV8.4 auditory nerve system    qh   ah
RT EV6 auditory sense    qh   ah
+GY8e language or speech disorder    qh   ah
GW10.4.6.  .  .  deafness   qh
GW12e.  olfactory system disorder   qh
BT+XV12e olfactory system    qh   ah
RT EV10 olfactory sense    qh   ah
+FG34e olfactory perception    qh   ah
+GW4e sensory nerve disorder    qh   ah
GW12.2.  .  anosmia   qh
GW12.4.  .  parosmia   qh
ST paraosmia

GXenervous system disorder   d-out   qh
ST neurologic disorders
BT+GK disorder by body system or organ function    qh   ah
+XWe nervous system    qh   ah
RT+EWe nervous system function    qh   ah
+FFe state of consciousness    qh   ah
+FH cognition, learning, and memory    qh   ah
+GL2 musculoskeletal symptom    qh   ah
+GZ2.10e cognitive and memory disorder    qh   ah
+HG22 nervous system diagnosis    qh   ah
GX2e.  PNS disorder   qh
ST peripheral nervous system disorder
GX2.2.  .  multiple sclerosis   qh
GX2.4.  .  myasthenia gravis   qh
BT+GU6e autoimmune disorder    qh   ah
GX2.6e.  .  neuropathy   qh
GX2.6.2.  .  .  peripheral neuropathy   qh
GX2.6.2.2e.  .  .  .  alcoholic polyneuropathy   qh
ST alcoholic neuropathy
alcoholic paralysis
alcoholic polyneuritis
BT+GD4 alcohol related disorder    qh   ah
RT+GZ6.2.6.4.4e Wernicke-Korsakoff psychosis    qh   ah
GX4e.  CNS disorder   qh
ST central nervous system disorders
NT+GX6.18 extrapyramidal disorder    qh   ah
+GZ6.2.6.6e organic brain syndrome    qh   ah
RT+EW12e CNS function    qh   ah
+GH6.2.6.10.2e brain injury    qh   ah
GX4.2.  .  headache, cephalalgia   qh
GX4.2.2e.  .  .  headache   qh
HN ETOH descriptor 1995.
BT+GFe symptom    qh   ah
GX4.2.2.4.  .  .  .  migraine headache   qh
GX4.2.4.  .  .  cephalalgia   qh
GX4.4e.  .  brain damage   qh
HN Introduced 1995.
RT+GH6.2.6.10.2e brain injury    qh   ah
GX4.4.2e.  .  .  AODR structural brain damage   qh
HN Introduced 2000.
ST AODR structural brain change
BT+GDe AODR disorder    qh   ah
RT+GD2e AODR mental disorder    qh   ah
GX4.6.  .  brain edema   qh
ST cerebral edema
GX4.8e.  .  brain atrophy   qh
ST cerebral atrophy
BT+GX6e CNS degenerative disorder    qh   ah
GX4.10.  .  hydrocephalus   qh
BT+GG12.4 abnormal accumulation of body fluid    qh   ah
RT XB2.6e cerebrospinal fluid    qh   ah
GX4.12e.  .  cerebral vascular disorder   qh
ST cerebrovascular disorders
NT+GH6.2.6.10e head injury    qh   ah
BT+GN10e vascular disorder    qh   ah
RT+GN6.10e vascular ischemia    qh   ah
+GZ6.2.4e dementia    qh   ah
GX4.12.2e.  .  .  stroke   qh
SN Any condition leading to partially or completely restricted blood flow to an organ; often used to denote blood loss to the brain. Stroke may be categorized as ischemic, in which blood vessel blockage has an etiology similar to that of coronary artery disorder, or hemorrhagic, in which bleeding through the vessel wall causes the loss of normal blood flow.
ST cerebral vascular accident
RT+GN10.2.2e hemorrhage    qh   ah
GX4.12.2.2.  .  .  .  cerebral ischemia or hypoxia   qh
BT+GF2.12e hypoxia    qh   ah
GX4.12.2.2.4.  .  .  .  .  transient cerebral ischemic attack   qh
ST cerebral vascular insufficiency
TIA
GX4.12.4e.  .  .  cerebral infarction   qh
HN Introduced 1995.
GX4.12.6e.  .  .  cerebral hemorrhage   qh
RT+GN10.2.2e hemorrhage    qh   ah
GX4.12.8.  .  .  cerebral hematoma   qh
RT GN10.2.4 hematoma    qh   ah
GX4.14e.  .  epilepsy   qh
ST epileptic seizure
RT+GF2.26e convulsion    qh   ah
GX4.16e.  .  CNS inflammation or infection   qh
ST central nervous system inflammation or infection
RT+GG16.6e infection    qh   ah
+GH16e communicable disease    qh   ah
GX4.16.2e.  .  .  encephalopathy   qh
ST brain dysfunction
RT+GH6.2.6.10.2e brain injury    qh   ah
GX4.16.2.2e.  .  .  .  Wernicke's encephalopathy   qh
HN Changed descriptor 2000; through 1999 use "Wernicke encephalopathy."
SN An acute, life-threatening, neurological syndrome consisting of confusion, apathy, dullness, a dreamy delirium, palsies of the ocular muscles and of gaze, nystagmus and disturbances in equilibrium, and ataxia. Its most common cause in industrialized countries is thiamine deficiency associated with alcoholism. If not treated immediately with thiamine, the patient is likely to die or progress into an amnesic syndrome.
ST other and unspecified manifestations of thiamine deficiency
other vitamin B1 deficiency states
Wernicke's disease
Wernicke's syndrome
BT+GD4 alcohol related disorder    qh   ah
+GH14.4.6.8e thiamine deficiency    qh   ah
RT GD4.2.2.8e alcoholic Korsakoff's syndrome    qh   ah
+GZ6.2.6.4e Korsakoff's syndrome    qh   ah
+GZ6.2.6.4.4e Wernicke-Korsakoff psychosis    qh   ah
GX4.16.2.4e.  .  .  .  hepatic encephalopathy   qh
SN A progressive metabolic liver disorder that affects intellectual functioning and is characterized by disturbances of consciousness that may progress to psychiatric changes or coma.
ST biliary encephalopathy
coma hepaticum
hepatic coma
hepatocerebral syndrome
portacaval encephalopathy
portal-systemic encephalopathy
RT GF2.28.10e coma    qh   ah
 GQ10.2.6e alcoholic liver cirrhosis    qh   ah
+GQ10.6e chronic liver disease    qh   ah
GX4.16.4.  .  .  encephalitis   qh
GX4.16.6.  .  .  encephalomyelitis   qh
HN Introduced 2000.
SN Inflammatory condition of the brain and spinal cord characterized by fever, headache, stiff neck, back pain, and vomiting.
NT GH16.12.2 chronic fatigue syndrome    qh   ah
GX4.16.8.  .  .  meningitis   qh
RT+GH16.12e viral disease    qh   ah
GX4.16.10.  .  .  brain abscess   qh
BT+GG16.6.2.2e abscess    qh   ah
GX4.16.12.  .  .  viral CNS infection   qh
NT GH16.12.10 poliomyelitis    qh   ah
 GH16.12.18 rabies    qh   ah
BT+GH16e communicable disease    qh   ah
GX4.16.14.  .  .  bacterial CNS infection   qh
BT+GH16e communicable disease    qh   ah
GX6e.  CNS degenerative disorder   qh
ST central nervous system degenerative disorder
NT GX4.8e brain atrophy    qh   ah
+GZ6.2.6.4e Korsakoff's syndrome    qh   ah
RT GZ6.2.4.2.2 presenile dementia    qh   ah
GX6.2e.  .  Alzheimer's disease   qh
RT+GZ6.2.4.2 senile dementia    qh   ah
 GZ6.2.4.2.2 presenile dementia    qh   ah
GX6.4.  .  Pick's disease   qh
GX6.6.  .  Creutzfeldt-Jakob's disease   qh
GX6.8.  .  Huntington's chorea   qh
GX6.10e.  .  Parkinson's disease   qh
RT+GX6.18 extrapyramidal disorder    qh   ah
GX6.12.  .  degenerative motor system disorder   qh
RT+GL2.2e abnormal involuntary movement    qh   ah
+GL2.4.4.2e ataxia    qh   ah
GX6.12.2.  .  .  amyotrophic lateral sclerosis   qh
BT+GX6.22e spinal cord disorder    qh   ah
GX6.14.  .  CNS demyelinating disorder   qh
GX6.14.2e.  .  .  Marchiafava-Bignami disease   qh
GX6.14.4e.  .  .  central pontine myelinosis   qh
HN ETOH descriptor 1995.
GX6.16.  .  spinocerebellar disorder   qh
ST ataxia telangiectasia
Friedrich's ataxia
GX6.16.2e.  .  .  cerebellar ataxia   qh
GX6.16.2.2e.  .  .  .  alcoholic cerebellar degeneration   qh
BT+GD4 alcohol related disorder    qh   ah
GX6.18.  .  extrapyramidal disorder   qh
BT+GX4e CNS disorder    qh   ah
RT GX6.10e Parkinson's disease    qh   ah
GX6.18.2.  .  .  chorea   qh
GX6.20.  .  myoclonus   qh
GX6.22e.  .  spinal cord disorder   qh
NT GX6.12.2 amyotrophic lateral sclerosis    qh   ah
BT+XZ6e spinal cord    qh   ah
GX6.22.2.  .  .  spinal cord injury   qh
BT+GH6.2e injury    qh   ah
GX6.22.2.2.  .  .  .  paraplegia   qh
GX6.22.2.4.  .  .  .  hemiplegia   qh
GX8.  congenital nervous system disorder   qh
ST tuberous sclerosis
BT+GJ4.2e congenital anomaly    qh   ah
GX8.2.  .  anencephaly   qh
RT+GJ2.16.2.4e alcohol-related intrauterine disorder    qh   ah

GYedisorder of higher mental process   d-out   qh
BT+GK disorder by body system or organ function    qh   ah
RT+F concepts in psychology and thought    qh   ah
 FB12.18e clinical psychology    qh   ah
+GZ2 mental symptom    qh   ah
+GZ2.4 perceptual disturbance    qh   ah
+GZ2.10e cognitive and memory disorder    qh   ah
GY2e.  developmental delay   qh
ST specific delays in development
specific developmental disorders
NT GZ12.4 hyperkinesis with developmental delay    qh   ah
RT+FCe psychological development    qh   ah
+GJe developmental disorder    qh   ah
 GZ2.6.8 psychomotor retardation    qh   ah
GY2.4e.  .  motor skills disorder   qh
RT+GL2.2e abnormal involuntary movement    qh   ah
GY2.4.2.  .  .  developmental coordination disorder   qh
RT+GL2.4.4.2e ataxia    qh   ah
GY4.  minimal brain dysfunction   qh
HN Introduced 2000.
RT+GZ12.2e attention deficit disorder    qh   ah
GY6e.  mental retardation   qh
SN Intellectual functioning that is two or more standard deviations below the mean (usually below 70 IQ range), concurrent with deficits in adaptive behavior, and manifested during the developmental period.
ST amentia
mental deficiency
mental subnormality
oligophrenia
RT+FEe intelligence and ability    qh   ah
+FE2e intellectual development    qh   ah
+FE4 intelligence    qh   ah
 GA2.8.2.4e mental disability    qh   ah
+GJ2.16.2.4e alcohol-related intrauterine disorder    qh   ah
+GJ4.2.10e neurodevelopmental anomaly    qh   ah
 GJ4.2.10.2e Down's syndrome    qh   ah
 TK4.4.6.2e mentally retarded    qh   ah
GY6.2.  .  mild mental retardation   qh
SN IQ 50-55 to 70. Mildly retarded, or educable, individuals are able to acquire functional academic skills through special education, and adults can usually maintain themselves at least semi-independently.
ST borderline mental retardation
GY6.4.  .  moderate mental retardation   qh
SN IQ 35-40 to 50-55. Moderately retarded, or trainable, individuals can learn self-help, communication, social, or simple vocational skills but only limited academic skills.
GY6.6.  .  severe mental retardation   qh
SN IQ 20-25 to 35-40. Severely retarded individuals require continual supervision and care.
GY6.8.  .  profound mental retardation   qh
SN IQ below 20-25.
GY8e.  language or speech disorder   qh
ST academic skills disorder
communication disorder
RT EN8 phonation    qh   ah
+FE6.2.2e language ability    qh   ah
+GW8.4e vision disorder    qh   ah
+GW10.4 hearing disorder    qh   ah
GY8.2.  .  language disorder   qh
ST language disability
language handicap
RT+FE6.2.2e language ability    qh   ah
 FE6.2.2.2 language development    qh   ah
GY8.2.4.  .  .  aphasia   qh
SN Impairment of the ability to comprehend or produce the symbols of spoken or written language due to brain dysfunction, not to mental or intellectual deficiency.
RT+GZ2.12e thought and speech disturbance    qh   ah
GY8.2.4.6.  .  .  .  global aphasia   qh
GY8.2.6.  .  .  reading disorder   qh
GY8.2.8.  .  .  writing disorder   qh
GY8.4.  .  speech disorder   qh
RT GZ2.12.12 slurred speech    qh   ah
GY8.4.2.  .  .  dysarthria   qh
RT+GL6e muscular disorder    qh   ah
GY8.4.4.  .  .  stuttering   qh
GY8.4.6.  .  .  articulation disorder   qh
GY10.  arithmetic disorder   qh
GY12.  cognitive motor disorder   qh
RT+GZ2.10e cognitive and memory disorder    qh   ah
GY14.  apraxia   qh


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