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 |
|---|---|---|---|---|
| Entropion The turning inward (inversion) of the edge of the eyelid, with the tarsal cartilage turned inward toward the eyeball. (Dorland, 27th ed) | Disorder | Pathology | Visual System [curated_secondary] | AMW:DIS:110071 |
| Enuresis Involuntary discharge of URINE after expected age of completed development of urinary control. This can happen during the daytime (DIURNAL ENURESIS) … | Disorder | Pathology | Renal and Urinary System [curated_secondary] | AMW:DIS:120179 |
| Environmental Illness A polysymptomatic condition believed by clinical ecologists to result from immune dysregulation induced by common foods, allergens, and chemicals, re… | Immune Disorder | Pathology | Immune System [curated_secondary] | AMW:DIS:200008 |
| Eosinophilia Abnormal increase of EOSINOPHILS in the blood, tissues or organs. | Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150119 |
| Eosinophilia-Myalgia Syndrome A complex systemic syndrome with inflammatory and autoimmune components that affect the skin, fascia, muscle, nerve, blood vessels, lung, and heart. … | Syndrome | Pathology | Musculoskeletal System [curated_secondary] | AMW:DIS:050247 |
| Eosinophilic Esophagitis Chronic ESOPHAGITIS characterized by esophageal mucosal EOSINOPHILIA. It is diagnosed when an increase in EOSINOPHILS are present over the entire eso… | Inflammatory Disorder | Pathology | Digestive System [curated_secondary] | AMW:DIS:060067 |
| Eosinophilic Granuloma The most benign and common form of Langerhans-cell histiocytosis which involves localized nodular lesions predominantly of the bones but also of the … | Pathologic Condition | Pathology | Musculoskeletal System [curated_secondary] | AMW:DIS:050092 |
| Epidermolysis Bullosa Group of genetically determined disorders characterized by the blistering of skin and mucosae. There are four major forms: acquired, simple, junction… | Congenital Disorder | Pathology | Integumentary System [curated_secondary] | AMW:DIS:160037 |
| Epidermolysis Bullosa Acquisita Form of epidermolysis bullosa characterized by trauma-induced, subepidermal blistering with no family history of the disease. Direct immunofluorescen… | Congenital Disorder | Pathology | Integumentary System [curated_secondary] | AMW:DIS:160038 |
| Epidermolysis Bullosa Dystrophica Form of epidermolysis bullosa characterized by atrophy of blistered areas, severe scarring, and nail changes. It is most often present at birth or in… | Congenital Disorder | Pathology | Integumentary System [curated_secondary] | AMW:DIS:160039 |
| Epidermolysis Bullosa Simplex A form of epidermolysis bullosa characterized by serous bullae that heal without scarring. Mutations in the genes that encode KERATIN-5 and KERATIN-1… | Congenital Disorder | Pathology | Integumentary System [curated_secondary] | AMW:DIS:160041 |
| Epidermolysis Bullosa, Junctional Form of epidermolysis bullosa having onset at birth or during the neonatal period and transmitted through autosomal recessive inheritance. It is char… | Congenital Disorder | Pathology | Integumentary System [curated_secondary] | AMW:DIS:160040 |
| Epididymitis Inflammation of the EPIDIDYMIS. Its clinical features include enlarged epididymis, a swollen SCROTUM; PAIN; PYURIA; and FEVER. It is usually related … | Inflammatory Disorder | Pathology | Reproductive System [curated_secondary] | AMW:DIS:120277 |
| Epilepsia Partialis Continua A variant of EPILEPSY characterized by continuous focal jerking of a body part over a period of hours, days, or even years without spreading to other… | Pathologic Condition | Pathology | Nervous System [curated_secondary] | AMW:DIS:100553 |
| Epilepsies, Myoclonic A clinically diverse group of epilepsy syndromes characterized either by myoclonic seizures or by myoclonus in association with other seizure types. … | Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100250 |
| Epilepsies, Partial Conditions characterized by recurrent paroxysmal neuronal discharges which arise from a focal region of the brain. Partial seizures are divided into … | Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100241 |
| Epilepsy A disorder characterized by recurrent episodes of paroxysmal brain dysfunction due to a sudden, disorderly, and excessive neuronal discharge. Epileps… | Neurologic Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100239 |
| Epilepsy, Absence A seizure disorder usually occurring in childhood characterized by rhythmic electrical brain discharges of generalized onset. Clinical features inclu… | Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100255 |
| Epilepsy, Benign Neonatal A condition marked by recurrent seizures that occur during the first 4-6 weeks of life despite an otherwise benign neonatal course. Autosomal dominan… | Congenital Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100248 |
| Epilepsy, Complex Partial A disorder characterized by recurrent partial seizures marked by impairment of cognition. During the seizure the individual may experience a wide var… | Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100242 |
| Epilepsy, Frontal Lobe A localization-related (focal) form of epilepsy characterized by seizures which arise in the FRONTAL LOBE. | Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100243 |
| Epilepsy, Generalized Recurrent conditions characterized by epileptic seizures which arise diffusely and simultaneously from both hemispheres of the brain. Classification … | Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100249 |
| Epilepsy, Partial, Motor A disorder characterized by recurrent localized paroxysmal discharges of cerebral neurons that give rise to seizures that have motor manifestations. … | Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100244 |
| Epilepsy, Partial, Sensory A disorder characterized by recurrent focal onset seizures which have sensory (i.e., olfactory, visual, tactile, gustatory, or auditory) manifestatio… | Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100245 |
| Epilepsy, Post-Traumatic Recurrent seizures causally related to CRANIOCEREBRAL TRAUMA. Seizure onset may be immediate but is typically delayed for several days after the inju… | Traumatic Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100145 |
| Epilepsy, Reflex A subtype of epilepsy characterized by seizures that are consistently provoked by a certain specific stimulus. Auditory, visual, and somatosensory st… | Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100259 |
| Epilepsy, Rolandic An autosomal dominant inherited partial epilepsy syndrome with onset between age 3 and 13 years. Seizures are characterized by PARESTHESIA and tonic … | Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100246 |
| Epilepsy, Temporal Lobe A localization-related (focal) form of epilepsy characterized by recurrent seizures that arise from foci within the TEMPORAL LOBE, most commonly from… | Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100247 |
| Epilepsy, Tonic-Clonic A generalized seizure disorder characterized by recurrent major motor seizures. The initial brief tonic phase is marked by trunk flexion followed by … | Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100256 |
| Epileptic Syndromes EPILEPTIC SEIZURES that are of similar type and age of onset and have other similar features (e.g., clinical course, EEG findings, genetic associatio… | Syndrome | Pathology | Nervous System [curated_secondary] | AMW:DIS:100260 |