Public registry
Nodes
Browse canonical concepts by label, domain, node type, prefix and encoded class.
Current membership scope: Base domain only
| Concept | Node type | Base domain | Matched membership | Identifier |
|---|---|---|---|---|
| Albuminuria The presence of albumin in the urine, an indicator of KIDNEY DISEASES. | Pathologic Condition | Pathology | Base domain | AMW:DIS:120187 |
| Alcohol Withdrawal Delirium An acute organic mental disorder induced by cessation or reduction in chronic alcohol consumption. Clinical characteristics include CONFUSION; DELUSI… | Toxic Disorder | Pathology | Base domain | AMW:DIS:100621 |
| Alcohol Withdrawal Seizures A condition where seizures occur in association with ethanol abuse (ALCOHOLISM) without other identifiable causes. Seizures usually occur within the … | Pathologic Condition | Pathology | Base domain | AMW:DIS:100549 |
| Alcohol-Induced Disorders Disorders stemming from the misuse and abuse of alcohol. | Toxic Disorder | Pathology | Base domain | AMW:DIS:250041 |
| Alcohol-Induced Disorders, Nervous System Acute and chronic neurologic disorders associated with the various neurologic effects of ETHANOL. Primary sites of injury include the brain and perip… | Toxic Disorder | Pathology | Base domain | AMW:DIS:100619 |
| Alcoholic Intoxication An acute brain syndrome which results from the excessive ingestion of ETHANOL or ALCOHOLIC BEVERAGES. | Toxic Disorder | Pathology | Base domain | AMW:DIS:250042 |
| Alcoholic Korsakoff Syndrome A neurological disorder characterized by inattentiveness and the inability to form short term memories. It is caused by THIAMINE DEFICIENCY due to ch… | Syndrome | Pathology | Base domain | AMW:DIS:100505 |
| Alcoholic Neuropathy A condition where damage to the peripheral nervous system (including the peripheral elements of the autonomic nervous system) is associated with chro… | Toxic Disorder | Pathology | Base domain | AMW:DIS:100612 |
| Alert Fatigue, Health Personnel Mental fatigue experienced by health care providers who encounter numerous alerts and reminders from the use of CLINICAL DECISION SUPPORT SYSTEMS. As… | Pathologic Condition | Pathology | Base domain | AMW:DIS:230248 |
| Aleutian Mink Disease A slow progressive disease of mink caused by the ALEUTIAN MINK DISEASE VIRUS. It is characterized by poor reproduction, weight loss, autoimmunity, hy… | Infectious Disorder | Pathology | Base domain | AMW:DIS:010666 |
| Alexander Disease Rare leukoencephalopathy with infantile-onset accumulation of Rosenthal fibers in the subpial, periventricular, and subependymal zones of the brain. … | Congenital Disorder | Pathology | Base domain | AMW:DIS:100082 |
| Alexia, Pure Loss of the power to comprehend written materials despite preservation of the ability to write (i.e., alexia without agraphia). This condition is gen… | Pathologic Condition | Pathology | Base domain | AMW:DIS:100459 |
| Alice in Wonderland Syndrome Neurological condition characterized by disturbances in VISUAL PERCEPTION, most often of BODY SCHEMA, TIME PERCEPTION and HALLUCINATIONS. It is assoc… | Syndrome | Pathology | Base domain | AMW:DIS:100267 |
| Alien Limb Phenomenon An apraxia characterized by the affected limb having involuntary, autonomous, and seemingly purposeful behaviors that are perceived as being controll… | Pathologic Condition | Pathology | Base domain | AMW:DIS:100518 |
| Aliivibrio Infections Infections with bacteria of the genus ALIIVIBRIO. | Infectious Disorder | Pathology | Base domain | AMW:DIS:010039 |
| Alkalosis A pathological condition that removes acid or adds base to the body fluids. | Metabolic Disorder | Pathology | Base domain | AMW:DIS:180008 |
| Alkalosis, Respiratory A state due to excess loss of carbon dioxide from the body. (Dorland, 27th ed) | Metabolic Disorder | Pathology | Base domain | AMW:DIS:080131 |
| Alkaptonuria An inborn error of amino acid metabolism resulting from a defect in the enzyme HOMOGENTISATE 1,2-DIOXYGENASE, an enzyme involved in the breakdown of … | Congenital Disorder | Pathology | Base domain | AMW:DIS:160073 |
| Allergic Fungal Sinusitis Fungal infection in the PARANASAL SINUSES characterized by common allergy respiratory symptoms, recurrent NASAL POLYPS and/or ASTHMA with buildup of … | Immune Disorder | Pathology | Base domain | AMW:DIS:010234 |
| Allesthesia A neurological disorder in which a sensory stimulus, usually tactile but more rarely other sensory modalities, is misperceived in a location distant … | Pathologic Condition | Pathology | Base domain | AMW:DIS:100510 |
| Alopecia Absence of hair from areas where it is normally present. | Pathologic Condition | Pathology | Base domain | AMW:DIS:170078 |
| Alopecia Areata Loss of scalp and body hair involving microscopically inflammatory patchy areas. | Disorder | Pathology | Base domain | AMW:DIS:170079 |
| alpha 1-Antitrypsin Deficiency Deficiency of the protease inhibitor ALPHA 1-ANTITRYPSIN that manifests primarily as PULMONARY EMPHYSEMA and LIVER CIRRHOSIS. | Congenital Disorder | Pathology | Base domain | AMW:DIS:060176 |
| alpha-Mannosidosis An inborn error of metabolism marked by a defect in the lysosomal isoform of ALPHA-MANNOSIDASE activity that results in lysosomal accumulation of man… | Congenital Disorder | Pathology | Base domain | AMW:DIS:160094 |
| alpha-Thalassemia A disorder characterized by reduced synthesis of the alpha chains of hemoglobin. The severity of this condition can vary from mild anemia to death, d… | Congenital Disorder | Pathology | Base domain | AMW:DIS:150023 |
| Alphavirus Infections Virus diseases caused by members of the ALPHAVIRUS genus of the family TOGAVIRIDAE. | Infectious Disorder | Pathology | Base domain | AMW:DIS:010616 |
| Alstrom Syndrome Rare autosomal recessive disease characterized by multiple organ dysfunction. The key clinical features include retinal degeneration (NYSTAGMUS, PATH… | Syndrome | Pathology | Base domain | AMW:DIS:100383 |
| Alternariosis Opportunistic fungal infection by a member of ALTERNARIA genus. | Infectious Disorder | Pathology | Base domain | AMW:DIS:010257 |
| Altitude Sickness Multiple symptoms associated with reduced oxygen at high ALTITUDE. | Exposure Related Disorder | Pathology | Base domain | AMW:DIS:080117 |
| Alveolar Bone Loss Resorption or wasting of the tooth-supporting bone (ALVEOLAR PROCESS) in the MAXILLA or MANDIBLE. | Disorder | Pathology | Base domain | AMW:DIS:050088 |