Public registry
Nodes
Browse canonical concepts by label, domain, node type, prefix and encoded class.
Current membership scope: Domain and all descendants
| Concept | Node type | Base domain | Matched membership | Identifier |
|---|---|---|---|---|
| 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 | Nervous System [curated_secondary], Neurology [curated_secondary] | AMW:DIS:100510 |
| Alopecia Absence of hair from areas where it is normally present. | Pathologic Condition | Pathology | Dermatology [curated_secondary], Integumentary System [curated_secondary] | AMW:DIS:170078 |
| Alopecia Areata Loss of scalp and body hair involving microscopically inflammatory patchy areas. | Disorder | Pathology | Dermatology [curated_secondary], Integumentary System [curated_secondary] | 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 | Digestive System [curated_secondary], Gastroenterology [curated_secondary] | 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 | Clinical Genetics [curated_secondary] | 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 | Haematology [curated_secondary], Hematopoietic System [curated_secondary] | AMW:DIS:150023 |
| Alphavirus Infections Virus diseases caused by members of the ALPHAVIRUS genus of the family TOGAVIRIDAE. | Infectious Disorder | Pathology | Infectious Diseases [curated_secondary] | 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 | Nervous System [curated_secondary], Neurology [curated_secondary] | AMW:DIS:100383 |
| Altered Mental Status Altered mental status used as a ClinicalGraph target concept for clinical_medicine / symptom. | Symptom | Clinical Medicine | Clinical Medicine [base] | AMW:SYM:165005 |
| Altered Taste Created as a target node for a staged ClinicalGraph edge. Review and enrich this node later if needed. | Symptom | Clinical Medicine | Clinical Medicine [base], Respiratory System [role_derived] | AMW:SYM:175007 |
| Alternariosis Opportunistic fungal infection by a member of ALTERNARIA genus. | Infectious Disorder | Pathology | Infectious Diseases [curated_secondary] | AMW:DIS:010257 |
| Altitude Sickness Multiple symptoms associated with reduced oxygen at high ALTITUDE. | Exposure Related Disorder | Pathology | Respiratory Medicine [curated_secondary], Respiratory System [curated_secondary] | AMW:DIS:080117 |
| Alveolar Bone Loss Resorption or wasting of the tooth-supporting bone (ALVEOLAR PROCESS) in the MAXILLA or MANDIBLE. | Disorder | Pathology | Dentistry [curated_secondary], Musculoskeletal System [curated_secondary] | AMW:DIS:050088 |
| Alveolar Inflammatory Exudate Created as a target node for a staged ClinicalGraph edge. Review and enrich this node later if needed. | Pathological finding | Pathology | Respiratory System [role_derived] | AMW:FIND:150005 |
| Alveolitis, Extrinsic Allergic A common interstitial lung disease caused by hypersensitivity reactions of PULMONARY ALVEOLI after inhalation of and sensitization to environmental a… | Immune Disorder | Pathology | Respiratory Medicine [curated_secondary], Respiratory System [curated_secondary] | AMW:DIS:080047 |
| Alzheimer Disease A degenerative disease of the BRAIN characterized by the insidious onset of DEMENTIA. Impairment of MEMORY, judgment, attention span, and problem sol… | Disorder | Pathology | Nervous System [curated_secondary], Neurology [curated_secondary], Psychiatry [curated_secondary] | AMW:DIS:100227 |
| Amaurosis Fugax Transient complete or partial monocular blindness due to retinal ischemia. This may be caused by emboli from the CAROTID ARTERY (usually in associati… | Pathologic Condition | Pathology | Nervous System [curated_secondary], Neurology [curated_secondary] | AMW:DIS:100567 |
| Amblyopia A nonspecific term referring to impaired vision. Major subcategories include stimulus deprivation-induced amblyopia and toxic amblyopia. Stimulus dep… | Pathologic Condition | Pathology | Nervous System [curated_secondary], Neurology [curated_secondary] | AMW:DIS:100050 |
| Ambulatory Care Sensitive Conditions Various health conditions in OUTPATIENT CARE settings for which adequate management, treatment and interventions delivered in the ambulatory care set… | Epidemiologic measure | Community Medicine | Community Medicine [base] | AMW:TECH:050269 |
| Amebiasis Infection with any of various amebae. It is an asymptomatic carrier state in most individuals, but diseases ranging from chronic, mild diarrhea to fu… | Infectious Disorder | Pathology | Infectious Diseases [curated_secondary] | AMW:DIS:010503 |
| Ameloblastoma An immature epithelial tumor of the JAW originating from the epithelial rests of Malassez or from other epithelial remnants of the ENAMEL from the de… | Neoplastic Disorder | Pathology | Oncology [curated_secondary] | AMW:DIS:040471 |
| Amelogenesis Imperfecta A clinically and genetically heterogeneous group of hereditary conditions characterized by malformed DENTAL ENAMEL, usually involving DENTAL ENAMEL H… | Congenital Disorder | Pathology | Dentistry [curated_secondary] | AMW:DIS:070099 |
| Amenorrhea Absence of menstruation. | Pathologic Condition | Pathology | Gynaecology [curated_secondary], Reproductive System [curated_secondary] | AMW:DIS:230178 |
| Amino Acid Metabolism, Inborn Errors Disorders affecting amino acid metabolism. The majority of these disorders are inherited and present in the neonatal period with metabolic disturbanc… | Congenital Disorder | Pathology | Clinical Genetics [curated_secondary] | AMW:DIS:160072 |
| Amino Acid Transport Disorders, Inborn Disorders characterized by defective transport of amino acids across cell membranes. These include deficits in transport across brush-border epitheli… | Congenital Disorder | Pathology | Clinical Genetics [curated_secondary] | AMW:DIS:160080 |
| Aminoglycoside Antibiotic Exposure Exposure to an aminoglycoside antibiotic with potential renal or auditory toxicity. | Risk Factor | Clinical Medicine | Clinical Medicine [assigned] | AMW:RISK:135011 |
| Amnesia Pathologic partial or complete loss of the ability to recall past experiences (AMNESIA, RETROGRADE) or to form new memories (AMNESIA, ANTEROGRADE). T… | Pathologic Condition | Pathology | Nervous System [curated_secondary], Neurology [curated_secondary] | AMW:DIS:100501 |
| Amnesia, Anterograde Loss of the ability to form new memories beyond a certain point in time. This condition may be organic or psychogenic in origin. Organically induced … | Pathologic Condition | Pathology | Nervous System [curated_secondary], Neurology [curated_secondary] | AMW:DIS:100502 |
| Amnesia, Retrograde Loss of the ability to recall information that had been previously encoded in memory prior to a specified or approximate point in time. This process … | Pathologic Condition | Pathology | Nervous System [curated_secondary], Neurology [curated_secondary] | AMW:DIS:100503 |
| Amnesia, Transient Global A syndrome characterized by a transient loss of the ability to form new memories. It primarily occurs in middle aged or elderly individuals, and epis… | Pathologic Condition | Pathology | Nervous System [curated_secondary], Neurology [curated_secondary] | AMW:DIS:100051 |