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 |
|---|---|---|---|---|
| Craniocerebral Trauma Traumatic injuries involving the cranium and intracranial structures (i.e., BRAIN; CRANIAL NERVES; MENINGES; and other structures). Injuries may be c… | Traumatic Disorder | Pathology | Base domain | AMW:DIS:100651 |
| Craniofacial Abnormalities Congenital structural deformities, malformations, or other abnormalities of the cranium and facial bones. | Congenital Disorder | Pathology | Base domain | AMW:DIS:050307 |
| Craniofacial Dysostosis Autosomal dominant CRANIOSYNOSTOSIS with shallow ORBITS; EXOPHTHALMOS; and maxillary hypoplasia. | Congenital Disorder | Pathology | Base domain | AMW:DIS:050016 |
| Craniofacial Fibrous Dysplasia Mostly benign fibro-osseous proliferation of the facial bones and skull. It can be either monostotic (localized to a single bone) or polyostotic (loc… | Pathologic Condition | Pathology | Base domain | AMW:DIS:050047 |
| Craniomandibular Disorders Diseases or disorders of the muscles of the head and neck, with special reference to the masticatory muscles. The most notable examples are TEMPOROMA… | Disorder | Pathology | Base domain | AMW:DIS:050182 |
| Craniopharyngioma A benign pituitary-region neoplasm that originates from Rathke's pouch. The two major histologic and clinical subtypes are adamantinous (or classical… | Neoplastic Disorder | Pathology | Base domain | AMW:DIS:040252 |
| Craniosynostoses Premature closure of one or more CRANIAL SUTURES. It often results in plagiocephaly. Craniosynostoses that involve multiple sutures are sometimes ass… | Congenital Disorder | Pathology | Base domain | AMW:DIS:050027 |
| CREST Syndrome A mild form of LIMITED SCLERODERMA, a multi-system disorder. Its features include symptoms of CALCINOSIS; RAYNAUD DISEASE; ESOPHAGEAL MOTILITY DISORD… | Syndrome | Pathology | Base domain | AMW:DIS:060053 |
| Creutzfeldt-Jakob Syndrome A rare transmissible encephalopathy most prevalent between the ages of 50 and 70 years. Affected individuals may present with sleep disturbances, per… | Syndrome | Pathology | Base domain | AMW:DIS:010343 |
| Cri-du-Chat Syndrome An infantile syndrome characterized by a cat-like cry, failure to thrive, microcephaly, MENTAL RETARDATION, spastic quadriparesis, micro- and retrogn… | Syndrome | Pathology | Base domain | AMW:DIS:100486 |
| Cribriform Tissue Architecture Epithelial proliferation containing multiple punched-out luminal spaces. | Microscopic feature | Pathology | Base domain | AMW:FIND:210004 |
| Crigler-Najjar Syndrome A familial form of congenital hyperbilirubinemia transmitted as an autosomal recessive trait. It is characterized by icterus and brain damage caused … | Syndrome | Pathology | Base domain | AMW:DIS:160105 |
| Crisscross Heart A developmental malformation of the heart characterized by a twisted but not defective atrioventicular connection. The abnormal rotation of the ventr… | Congenital Disorder | Pathology | Base domain | AMW:DIS:140014 |
| Critical Illness A disease or state in which death is possible or imminent. | Pathologic Condition | Pathology | Base domain | AMW:DIS:230100 |
| Crohn Disease A chronic transmural inflammation that may involve any part of the DIGESTIVE TRACT from MOUTH to ANUS, mostly found in the ILEUM, the CECUM, and the … | Disorder | Pathology | Base domain | AMW:DIS:060099 |
| Cronkhite-Canada Syndrome A nonfamilial polyposis syndrome that is characterized by the presence of diffuse gastrointestinal polyposis, skin hyperpigmentation, ALOPECIA; DIARR… | Syndrome | Pathology | Base domain | AMW:DIS:060139 |
| Cross Infection Any infection which a patient contracts in a health-care institution. | Infectious Disorder | Pathology | Base domain | AMW:DIS:010379 |
| Croup Inflammation involving the GLOTTIS or VOCAL CORDS and the subglottic larynx. Croup is characterized by a barking cough, HOARSENESS, and persistent in… | Disorder | Pathology | Base domain | AMW:DIS:080027 |
| Crush Injuries Excessive compression of parts of the body that causes muscle swelling, fracture, and/or neurological disturbances in the affected areas. Crush injur… | Traumatic Disorder | Pathology | Base domain | AMW:DIS:260034 |
| Crush Syndrome Severe systemic manifestation of trauma and ischemia involving soft tissues, principally skeletal muscle, due to prolonged severe crushing. It leads … | Syndrome | Pathology | Base domain | AMW:DIS:260035 |
| Cryoglobulinemia A condition characterized by the presence of abnormal quantities of CRYOGLOBULINS in the blood. Upon cold exposure, these abnormal proteins precipita… | Immune Disorder | Pathology | Base domain | AMW:DIS:140257 |
| Cryopyrin-Associated Periodic Syndromes A group of rare autosomal dominant diseases, commonly characterized by atypical URTICARIA (hives) with systemic symptoms that develop into end-organ … | Syndrome | Pathology | Base domain | AMW:DIS:160064 |
| Crypt Abscesses Crypt abscesses used as a ClinicalGraph target concept for pathology / pathological_finding. | Pathological finding | Pathology | Base domain | AMW:FIND:150012 |
| Cryptococcosis Fungal infection caused by genus CRYPTOCOCCUS. | Infectious Disorder | Pathology | Base domain | AMW:DIS:010252 |
| Cryptogenic Organizing Pneumonia An interstitial lung disease of unknown etiology, occurring between 21-80 years of age. It is characterized by a dramatic onset of a pneumonia-like i… | Disorder | Pathology | Base domain | AMW:DIS:080018 |
| Cryptorchidism A developmental defect in which a TESTIS or both TESTES failed to descend from high in the ABDOMEN to the bottom of the SCROTUM. Testicular descent i… | Congenital Disorder | Pathology | Base domain | AMW:DIS:120302 |
| Cryptosporidiosis Intestinal infection with organisms of the genus CRYPTOSPORIDIUM. It occurs in both animals and humans. Symptoms include severe DIARRHEA. | Infectious Disorder | Pathology | Base domain | AMW:DIS:010483 |
| Crystal Arthropathies Joint disorders that are characterized by accumulation of microcrystals in and around the joint including in the SYNOVIAL FLUID. They are classified … | Disorder | Pathology | Base domain | AMW:DIS:050218 |
| Cubital Tunnel Syndrome Compression of the ULNAR NERVE in the cubital tunnel, which is formed by the two heads of the flexor carpi ulnaris muscle, humeral-ulnar aponeurosis,… | Syndrome | Pathology | Base domain | AMW:DIS:100599 |
| Cumulative Trauma Disorders Harmful and painful condition caused by overuse or overexertion of some part of the musculoskeletal system, often resulting from work-related physica… | Traumatic Disorder | Pathology | Base domain | AMW:DIS:260107 |