Public registry
Nodes
Browse canonical concepts by label, domain, node type, prefix and encoded class.
Current membership scope: Any direct membership
| Concept | Node type | Base domain | Matched membership | Identifier |
|---|---|---|---|---|
| alpha 1-Antitrypsin Deficiency Deficiency of the protease inhibitor ALPHA 1-ANTITRYPSIN that manifests primarily as PULMONARY EMPHYSEMA and LIVER CIRRHOSIS. | Congenital Disorder | Pathology | Pathology [base] | 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 | Pathology [base] | 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 | Pathology [base] | AMW:DIS:150023 |
| Alphavirus Infections Virus diseases caused by members of the ALPHAVIRUS genus of the family TOGAVIRIDAE. | Infectious Disorder | Pathology | Pathology [base] | 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 | Pathology [base] | AMW:DIS:100383 |
| Alternariosis Opportunistic fungal infection by a member of ALTERNARIA genus. | Infectious Disorder | Pathology | Pathology [base] | AMW:DIS:010257 |
| Altitude Sickness Multiple symptoms associated with reduced oxygen at high ALTITUDE. | Exposure Related Disorder | Pathology | Pathology [base] | AMW:DIS:080117 |
| Alveolar Bone Loss Resorption or wasting of the tooth-supporting bone (ALVEOLAR PROCESS) in the MAXILLA or MANDIBLE. | Disorder | Pathology | Pathology [base] | 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 | Pathology [base] | 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 | Pathology [base] | 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 | Pathology [base] | 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 | Pathology [base] | 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 | Pathology [base] | 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… | Pathologic Condition | Pathology | Pathology [base] | AMW:DIS:230093 |
| 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 | Pathology [base] | 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 | Pathology [base] | 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 | Pathology [base] | AMW:DIS:070099 |
| Amenorrhea Absence of menstruation. | Pathologic Condition | Pathology | Pathology [base] | 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 | Pathology [base] | 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 | Pathology [base] | AMW:DIS:160080 |
| 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 | Pathology [base] | 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 | Pathology [base] | 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 | Pathology [base] | 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 | Pathology [base] | AMW:DIS:100051 |
| Amniotic Band Syndrome A disorder present in the newborn infant in which constriction rings or bands, causing soft tissue depressions, encircle digits, extremities, or limb… | Syndrome | Pathology | Pathology [base] | AMW:DIS:160159 |
| Amphetamine-Related Disorders Disorders related or resulting from use of amphetamines. | Mental Disorder | Psychiatry | Pathology [curated_secondary] | AMW:PSY:030095 |
| Amputation, Traumatic Loss of a limb or other bodily appendage by accidental injury. | Traumatic Disorder | Pathology | Pathology [base] | AMW:DIS:260004 |
| Amyloid Fibril Deposition Extracellular accumulation of insoluble misfolded protein fibrils in beta-sheet configuration. | Pathological process | Pathology | Pathology [assigned] | AMW:PROC:135046 |
| Amyloid Neuropathies Disorders of the peripheral nervous system associated with the deposition of AMYLOID in nerve tissue. Familial, primary (nonfamilial), and secondary … | Metabolic Disorder | Pathology | Pathology [base] | AMW:DIS:100581 |
| Amyloid Neuropathies, Familial Inherited disorders of the peripheral nervous system associated with the deposition of AMYLOID in nerve tissue. The different clinical types based on… | Congenital Disorder | Pathology | Pathology [base] | AMW:DIS:100416 |