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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 |
|---|---|---|---|---|
| Common Bile Duct Diseases Diseases of the COMMON BILE DUCT including the AMPULLA OF VATER and the SPHINCTER OF ODDI. | Disorder | Pathology | Digestive System [curated_secondary] | AMW:DIS:060014 |
| Common Variable Immunodeficiency Heterogeneous group of immunodeficiency syndromes characterized by hypogammaglobulinemia of most isotypes, variable B-cell defects, and the presence … | Immune Disorder | Pathology | Immune System [curated_secondary] | AMW:DIS:200031 |
| Commotio Cordis A sudden CARDIAC ARRHYTHMIA (e.g., VENTRICULAR FIBRILLATION) caused by a blunt, non-penetrating impact to the precordial region of chest wall. Commot… | Traumatic Disorder | Pathology | Cardiovascular System [curated_secondary] | AMW:DIS:140064 |
| Compartment Syndromes Conditions in which increased pressure within a limited space compromises the BLOOD CIRCULATION and function of tissue within that space. Some of the… | Syndrome | Pathology | Musculoskeletal System [curated_secondary] | AMW:DIS:050243 |
| Complex Regional Pain Syndromes Conditions characterized by pain involving an extremity or other body region, HYPERESTHESIA, and localized autonomic dysfunction following injury to … | Syndrome | Pathology | Nervous System [curated_secondary] | AMW:DIS:100029 |
| Cone Dystrophy A general term which describes a group of rare eye disorders that affect the cone cells of the RETINA. Cone dystrophy can cause a variety of symptoms… | Disorder | Pathology | Visual System [curated_secondary] | AMW:DIS:110047 |
| Cone-Rod Dystrophies Genetically heterogeneous and sometimes syndromic (e.g., BARDET BIEDL SYNDROME; and SPINOCEREBELLAR ATAXIA TYPE 7) retinopathies with initial RETINAL… | Congenital Disorder | Pathology | Visual System [curated_secondary] | AMW:DIS:110048 |
| Confusion Primarily an observable or examinable clinical manifestation rather than a disease entity. | Clinical Sign | Clinical Medicine | Nervous System [curated_secondary] | AMW:SIGN:145027 |
| Congenital Bone Marrow Failure Syndromes Inherited syndromes characterized by deficiency or absence of various blood cells due to mutations that affect HEMATOPOIETIC STEM CELLS development a… | Syndrome | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150098 |
| Congenital Cranial Dysinnervation Disorders Congenital neurodevelopmental diseases characterized by abnormal eye, eyelid, and facial movements. Congenital cranial dysinnervation disorders (CCDD… | Congenital Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100354 |
| Congenital Hyperinsulinism A familial, nontransient HYPOGLYCEMIA with defects in negative feedback of GLUCOSE-regulated INSULIN release. Clinical phenotypes include HYPOGLYCEMI… | Congenital Disorder | Pathology | Digestive System [curated_secondary] | AMW:DIS:060219 |
| Congenital Hypothyroidism A condition in infancy or early childhood due to an in-utero deficiency of THYROID HORMONES that can be caused by genetic or environmental factors, s… | Metabolic Disorder | Pathology | Musculoskeletal System [curated_secondary] | AMW:DIS:050010 |
| Congenital Portosystemic Shunt Congenital vascular malformation where the portal venous system blood (PORTAL SYSTEM) bypasses the liver sinusoids and drains into the systemic vein … | Congenital Disorder | Pathology | Cardiovascular System [curated_secondary] | AMW:DIS:140042 |
| Congenitally Corrected Transposition of the Great Arteries A rare heart defect that occurs when the HEART VENTRICLES and attached valves, the MITRAL VALVE and the TRICUSPID VALVE are reversed so that the AORT… | Congenital Disorder | Pathology | Cardiovascular System [curated_secondary] | AMW:DIS:140036 |
| Conjunctival Diseases Diseases involving the CONJUNCTIVA. | Disorder | Pathology | Visual System [curated_secondary] | AMW:DIS:110003 |
| Conjunctivitis INFLAMMATION of the CONJUNCTIVA. | Inflammatory Disorder | Pathology | Visual System [curated_secondary] | AMW:DIS:110004 |
| Conjunctivitis, Allergic Conjunctivitis due to hypersensitivity to various allergens. | Immune Disorder | Pathology | Visual System [curated_secondary] | AMW:DIS:110005 |
| Connective Tissue Diseases A heterogeneous group of disorders, some hereditary, others acquired, characterized by abnormal structure or function of one or more of the elements … | Disorder | Pathology | Immune System [curated_secondary], Musculoskeletal System [curated_secondary] | AMW:DIS:170002 |
| Consciousness Disorders Organic mental disorders in which there is impairment of the ability to maintain awareness of self and environment and to respond to environmental st… | Pathologic Condition | Pathology | Nervous System [curated_secondary] | AMW:DIS:100478 |
| Constipation Primarily a patient-reported sensation, complaint or symptom rather than a disease entity. | Symptom | Clinical Medicine | Digestive System [curated_secondary] | AMW:SYM:145023 |
| Contracture Prolonged shortening of the muscle or other soft tissue around a joint, preventing movement of the joint. | Disorder | Pathology | Musculoskeletal System [curated_secondary] | AMW:DIS:050215 |
| Contrecoup Injury An injury in which the damage is located on the opposite side of the primary impact site. A blow to the back of head which results in contrecoup inju… | Traumatic Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100669 |
| Coproporphyria, Hereditary An autosomal dominant porphyria that is due to a deficiency of COPROPORPHYRINOGEN OXIDASE in the LIVER, the sixth enzyme in the 8-enzyme biosynthetic… | Congenital Disorder | Pathology | Digestive System [curated_secondary] | AMW:DIS:060211 |
| Cor Triatriatum A malformation of the heart in which the embryonic common PULMONARY VEIN was not incorporated into the LEFT ATRIUM leaving behind a perforated fibrom… | Congenital Disorder | Pathology | Cardiovascular System [curated_secondary] | AMW:DIS:140009 |
| Corneal Diseases Diseases of the cornea. | Disorder | Pathology | Visual System [curated_secondary] | AMW:DIS:110012 |
| Corneal Dystrophies, Hereditary Bilateral hereditary disorders of the cornea, usually autosomal dominant, which may be present at birth but more frequently develop during adolescenc… | Congenital Disorder | Pathology | Visual System [curated_secondary] | AMW:DIS:110013 |
| Corneal Dystrophy, Juvenile Epithelial of Meesmann An autosomal dominant form of hereditary corneal dystrophy due to a defect in cornea-specific KERATIN formation. Mutations in the genes that encode K… | Congenital Disorder | Pathology | Visual System [curated_secondary] | AMW:DIS:110014 |
| Corneal Edema Residual high-priority semantic candidate found after excluding all completed reclassification sources. | Clinical Sign | Clinical Medicine | Visual System [curated_secondary] | AMW:SIGN:175021 |
| Corneal Endothelial Cell Loss Residual high-priority semantic candidate found after excluding all completed reclassification sources. | Finding | Pathology | Visual System [curated_secondary] | AMW:FIND:159011 |
| Corneal Injuries Damage or trauma inflicted to the CORNEA by external means. | Traumatic Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100655 |