Public registry
Nodes
Browse canonical concepts by label, domain, node type, prefix and encoded class.
| Concept | Node type | Base domain | Identifier |
|---|---|---|---|
| Aphasia, Primary Progressive A progressive form of dementia characterized by the global loss of language abilities and initial preservation of other cognitive functions. Fluent a… | Pathologic Condition | Pathology | AMW:DIS:100228 |
| Aphasia, Wernicke Impairment in the comprehension of speech and meaning of words, both spoken and written, and of the meanings conveyed by their grammatical relationsh… | Pathologic Condition | Pathology | AMW:DIS:100466 |
| Aphonia Complete loss of phonation due to organic disease of the larynx or to nonorganic (i.e., psychogenic) causes. | Pathologic Condition | Pathology | AMW:DIS:080034 |
| Apical Hypertrophic Cardiomyopathy A hypertrophic cardiomyopathy characterized by apical hypertrophy, typically LEFT VENTRICULAR HYPERTROPHY (described as ace of spades sign), and deep… | Disorder | Pathology | AMW:DIS:140102 |
| Apnea A transient absence of spontaneous respiration. | Pathologic Condition | Pathology | AMW:DIS:080118 |
| Appendiceal Luminal Obstruction Appendiceal luminal obstruction used as a ClinicalGraph target concept for pathology / pathological_process. | Pathological process | Pathology | AMW:PROC:145007 |
| Appendiceal Neoplasms Tumors or cancer of the APPENDIX. | Neoplastic Disorder | Pathology | AMW:DIS:040508 |
| Appendicitis Acute inflammation of the APPENDIX. Acute appendicitis is classified as simple, gangrenous, or perforated. | Inflammatory Disorder | Pathology | AMW:DIS:010401 |
| Apraxia, Ideomotor A form of apraxia characterized by an acquired inability to carry out a complex motor activity despite the ability to mentally formulate the action. … | Pathologic Condition | Pathology | AMW:DIS:100519 |
| Apraxias A group of cognitive disorders characterized by the inability to perform previously learned skills that cannot be attributed to deficits of motor or … | Pathologic Condition | Pathology | AMW:DIS:100517 |
| Apudoma A general term collectively applied to tumors associated with the APUD CELLS series, irrespective of their specific identification. | Neoplastic Disorder | Pathology | AMW:DIS:040279 |
| Arachnodactyly An abnormal bone development that is characterized by extra long and slender hands and fingers, such that the clenched thumb extends beyond the ulnar… | Congenital Disorder | Pathology | AMW:DIS:050328 |
| Arachnoid Cysts Intracranial or spinal cavities containing a cerebrospinal-like fluid, the wall of which is composed of arachnoidal cells. They are most often develo… | Neoplastic Disorder | Pathology | AMW:DIS:040003 |
| Arachnoiditis Acute or chronic inflammation of the arachnoid membrane of the meninges most often involving the spinal cord or base of the brain. This term generall… | Inflammatory Disorder | Pathology | AMW:DIS:100427 |
| Arbovirus Infections Infections caused by arthropod-borne viruses, general or unspecified. | Infectious Disorder | Pathology | AMW:DIS:010614 |
| Arcus Senilis A corneal disease in which there is a deposition of phospholipid and cholesterol in the corneal stroma and anterior sclera. | Disorder | Pathology | AMW:DIS:110020 |
| Arenaviridae Infections Virus diseases caused by the ARENAVIRIDAE. | Infectious Disorder | Pathology | AMW:DIS:010690 |
| Argininosuccinic Aciduria Rare autosomal recessive disorder of the urea cycle which leads to the accumulation of argininosuccinic acid in body fluids and severe HYPERAMMONEMIA… | Congenital Disorder | Pathology | AMW:DIS:100125 |
| Argyria A permanent ashen-gray discoloration of the skin, conjunctiva, and internal organs resulting from long-continued use of silver salts. (Dorland, 27th … | Toxic Disorder | Pathology | AMW:DIS:170103 |
| Arm Injuries General or unspecified injuries involving the UPPER ARM and the FOREARM. | Traumatic Disorder | Pathology | AMW:DIS:260006 |
| Arnold-Chiari Malformation A group of congenital malformations involving the brainstem, cerebellum, upper spinal cord, and surrounding bony structures. Type II is the most comm… | Congenital Disorder | Pathology | AMW:DIS:100403 |
| Arrhythmia, Sinus Irregular HEART RATE caused by abnormal function of the SINOATRIAL NODE. It is characterized by a greater than 10% change between the maximum and the… | Pathologic Condition | Pathology | AMW:DIS:140054 |
| Arrhythmias, Cardiac Any disturbances of the normal rhythmic beating of the heart or MYOCARDIAL CONTRACTION. Cardiac arrhythmias can be classified by the abnormalities in… | Pathologic Condition | Pathology | AMW:DIS:140053 |
| Arrhythmogenic Right Ventricular Dysplasia A congenital cardiomyopathy that is characterized by infiltration of adipose and fibrous tissue into the RIGHT VENTRICLE wall and loss of myocardial … | Pathologic Condition | Pathology | AMW:DIS:140006 |
| Arsenic Poisoning Disorders associated with acute or chronic exposure to compounds containing ARSENIC (ARSENICALS) which may be fatal. Acute oral ingestion is associat… | Toxic Disorder | Pathology | AMW:DIS:100623 |
| Arterial Bleeding Into Subarachnoid Space Arterial bleeding into subarachnoid space used as a ClinicalGraph target concept for pathology / pathological_process. | Pathological process | Pathology | AMW:PROC:125012 |
| Arterial Occlusion Of Cerebral Circulation Arterial occlusion of cerebral circulation used as a ClinicalGraph target concept for pathology / pathological_process. | Pathological process | Pathology | AMW:PROC:145011 |
| Arterial Occlusive Diseases Pathological processes which result in the partial or complete obstruction of ARTERIES. They are characterized by greatly reduced or absence of blood… | Disorder | Pathology | AMW:DIS:140223 |
| Arterio-Arterial Fistula Abnormal communication between two ARTERIES that may result from injury or occur as a congenital abnormality. | Pathologic Condition | Pathology | AMW:DIS:140050 |
| Arteriolar Remodeling Arteriolar remodeling used as a ClinicalGraph target concept for pathology / pathological_process. | Pathological process | Pathology | AMW:PROC:155001 |