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 |
|---|---|---|---|---|
| Cicatrix The fibrous tissue that replaces normal tissue during the process of WOUND HEALING. | Pathologic Condition | Pathology | Base domain | AMW:DIS:230128 |
| Cicatrix, Hypertrophic An elevated scar, resembling a KELOID, but which does not spread into surrounding tissues. It is formed by enlargement and overgrowth of cicatricial … | Pathologic Condition | Pathology | Base domain | AMW:DIS:230129 |
| Ciguatera Poisoning Poisoning caused by ingestion of SEAFOOD containing microgram levels of CIGUATOXINS. The poisoning is characterized by gastrointestinal, neurological… | Toxic Disorder | Pathology | Base domain | AMW:DIS:250021 |
| Ciliary Motility Disorders Conditions caused by abnormal CILIA movement in the body, usually causing KARTAGENER SYNDROME, chronic respiratory disorders, chronic SINUSITIS, and … | Functional Disorder | Pathology | Base domain | AMW:DIS:080020 |
| Ciliopathies Genetic disorders caused by defects in genes related to the primary CILIUM; BASAL BODY; or CENTROSOME. Primary features may include obesity, SKELETAL… | Congenital Disorder | Pathology | Base domain | AMW:DIS:160008 |
| Ciliophora Infections Infections with protozoa of the phylum CILIOPHORA. | Infectious Disorder | Pathology | Base domain | AMW:DIS:010505 |
| Circoviridae Infections Virus diseases caused by the CIRCOVIRIDAE. | Infectious Disorder | Pathology | Base domain | AMW:DIS:010638 |
| Citrullinemia A group of diseases related to a deficiency of the enzyme ARGININOSUCCINATE SYNTHASE which causes an elevation of serum levels of CITRULLINE. In neon… | Congenital Disorder | Pathology | Base domain | AMW:DIS:100127 |
| Civatte Body Eosinophilic apoptotic keratinocyte or colloid body located near the dermoepidermal junction. | Microscopic feature | Pathology | Base domain | AMW:FIND:220008 |
| Classical Lissencephalies and Subcortical Band Heterotopias Disorders comprising a spectrum of brain malformations representing the paradigm of a diffuse neuronal migration disorder. They result in cognitive i… | Congenital Disorder | Pathology | Base domain | AMW:DIS:100393 |
| Classical Swine Fever An acute, highly contagious disease affecting swine of all ages and caused by the CLASSICAL SWINE FEVER VIRUS. It has a sudden onset with high morbid… | Infectious Disorder | Pathology | Base domain | AMW:DIS:010707 |
| Cleft Lip Congenital defect in the upper lip where the maxillary prominence fails to merge with the merged medial nasal prominences. It is thought to be caused… | Congenital Disorder | Pathology | Base domain | AMW:DIS:070029 |
| Cleft Palate Congenital fissure of the soft and/or hard palate, due to faulty fusion. | Congenital Disorder | Pathology | Base domain | AMW:DIS:050174 |
| Cleidocranial Dysplasia Autosomal dominant syndrome in which there is delayed closing of the CRANIAL FONTANELLES; complete or partial absence of the collarbones (CLAVICLES);… | Pathologic Condition | Pathology | Base domain | AMW:DIS:050042 |
| Clinical Deterioration A critical disease progression, often measured by a set of clinical parameters, which activates HOSPITAL RAPID RESPONSE TEAM. | Pathologic Condition | Pathology | Base domain | AMW:DIS:230102 |
| Cloacal Exstrophy A rare congenital malformation that affects the development of the urinary, digestive, and REPRODUCTIVE SYSTEMS due to CLOACA malformations. In this … | Congenital Disorder | Pathology | Base domain | AMW:DIS:060032 |
| Clonal Neoplastic Proliferation Expansion of a neoplastic cell population derived from a common altered progenitor. | Pathological process | Pathology | Base domain | AMW:PROC:165002 |
| Clonorchiasis Infection of the biliary passages with CLONORCHIS SINENSIS, also called Opisthorchis sinensis. It may lead to inflammation of the biliary tract, prol… | Infectious Disorder | Pathology | Base domain | AMW:DIS:010470 |
| Clostridium Infections Infections with bacteria of the genus CLOSTRIDIUM and closely related CLOSTRIDIOIDES or reclassified members of Clostridium. | Infectious Disorder | Pathology | Base domain | AMW:DIS:010197 |
| Clubfoot A deformed foot in which the foot is plantarflexed, inverted, and adducted. | Congenital Disorder | Pathology | Base domain | AMW:DIS:050154 |
| Cluster Headache A primary headache disorder that is characterized by severe, strictly unilateral PAIN which is orbital, supraorbital, temporal or in any combination … | Disorder | Pathology | Base domain | AMW:DIS:100273 |
| Coagulation Protein Disorders Hemorrhagic and thrombotic disorders resulting from abnormalities or deficiencies of coagulation proteins. | Disorder | Pathology | Base domain | AMW:DIS:150062 |
| Coagulative Necrosis Necrosis in which tissue architecture is temporarily preserved by protein denaturation. | Pathological process | Pathology | Base domain | AMW:PROC:135027 |
| Cobblestone Lissencephaly The smooth pebbled appearance of the CEREBRAL CORTEX with a thickened cortex and reduced and abnormal white matter, which results from migration of h… | Congenital Disorder | Pathology | Base domain | AMW:DIS:100395 |
| Cocarcinogenesis The combination of two or more different factors in the production of cancer. | Neoplastic Disorder | Pathology | Base domain | AMW:DIS:040657 |
| Coccidioidal Meningitis Meningitis caused by a fungus of the genus COCCIDIOIDES, endemic to the SOUTHWESTERN UNITED STATES, south-central Washington State, and parts of Mexi… | Inflammatory Disorder | Pathology | Base domain | AMW:DIS:010249 |
| Coccidioidomycosis Infection with a fungus of the genus COCCIDIOIDES, endemic to the SOUTHWESTERN UNITED STATES. It is sometimes called valley fever but should not be c… | Infectious Disorder | Pathology | Base domain | AMW:DIS:010251 |
| Coccidiosis Protozoan infection found in animals and man. It is caused by several different genera of COCCIDIA. | Infectious Disorder | Pathology | Base domain | AMW:DIS:010506 |
| Cochlear Diseases Pathological processes of the snail-like structure (COCHLEA) of the inner ear (LABYRINTH) which can involve its nervous tissue, blood vessels, or flu… | Disorder | Pathology | Base domain | AMW:DIS:090030 |
| Cockayne Syndrome A syndrome characterized by multiple system abnormalities including DWARFISM; PHOTOSENSITIVITY DISORDERS; PREMATURE AGING; and HEARING LOSS. It is ca… | Syndrome | Pathology | Base domain | AMW:DIS:050009 |