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 |
|---|---|---|---|---|
| Conjunctival Neoplasms Tumors or cancer of the CONJUNCTIVA. | Neoplastic Disorder | Pathology | Base domain | AMW:DIS:040541 |
| Conjunctivitis INFLAMMATION of the CONJUNCTIVA. | Inflammatory Disorder | Pathology | Base domain | AMW:DIS:110004 |
| Conjunctivitis, Acute Hemorrhagic A highly contagious disease characterized by subconjunctival hemorrhage, sudden swelling of the eyelids and congestion, redness, and pain in the eye.… | Inflammatory Disorder | Pathology | Base domain | AMW:DIS:010387 |
| Conjunctivitis, Allergic Conjunctivitis due to hypersensitivity to various allergens. | Immune Disorder | Pathology | Base domain | AMW:DIS:110005 |
| Conjunctivitis, Bacterial Purulent infections of the conjunctiva by several species of gram-negative, gram-positive, or acid-fast organisms. Some of the more commonly found ge… | Inflammatory Disorder | Pathology | Base domain | AMW:DIS:010028 |
| Conjunctivitis, Inclusion An infection of the eyes characterized by the presence in conjunctival epithelial cells of inclusion bodies indistinguishable from those of trachoma.… | Inflammatory Disorder | Pathology | Base domain | AMW:DIS:010029 |
| Conjunctivitis, Viral Inflammation, often mild, of the conjunctiva caused by a variety of viral agents. Conjunctival involvement may be part of a systemic infection. | Inflammatory Disorder | Pathology | Base domain | AMW:DIS:010386 |
| 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 | Base domain | 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 | Base domain | AMW:DIS:100478 |
| Constriction, Pathologic The condition of an anatomical structure's being constricted beyond normal dimensions. | Pathologic Condition | Pathology | Base domain | AMW:DIS:230012 |
| Continuous Colonic Mucosal Inflammation Continuous colonic mucosal inflammation used as a ClinicalGraph target concept for pathology / pathological_process. | Pathological process | Pathology | Base domain | AMW:PROC:105014 |
| Contracture Prolonged shortening of the muscle or other soft tissue around a joint, preventing movement of the joint. | Disorder | Pathology | Base domain | 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 | Base domain | AMW:DIS:100669 |
| Contusions Injuries resulting in hemorrhage, usually manifested in the skin. | Traumatic Disorder | Pathology | Base domain | AMW:DIS:260116 |
| Convalescence The period of recovery following an illness. | Pathologic Condition | Pathology | Base domain | AMW:DIS:230099 |
| Copper-Associated Hepatic Pigment Coarse granular copper-associated material identified in hepatocytes. | Microscopic feature | Pathology | Base domain | AMW:FIND:240007 |
| 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 | Base domain | 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 | Base domain | AMW:DIS:140009 |
| Corneal Diseases Diseases of the cornea. | Disorder | Pathology | Base domain | 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 | Base domain | 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 | Base domain | AMW:DIS:110014 |
| Corneal Endothelial Cell Loss Residual high-priority semantic candidate found after excluding all completed reclassification sources. | Finding | Pathology | Base domain | AMW:FIND:159011 |
| Corneal Injuries Damage or trauma inflicted to the CORNEA by external means. | Traumatic Disorder | Pathology | Base domain | AMW:DIS:100655 |
| Corneal Neovascularization New blood vessels originating from the corneal blood vessels and extending from the limbus into the adjacent CORNEAL STROMA. Neovascularization in th… | Vascular Disorder | Pathology | Base domain | AMW:DIS:110018 |
| Corneal Opacity Disorder occurring in the central or peripheral area of the cornea. The usual degree of transparency becomes relatively opaque. | Disorder | Pathology | Base domain | AMW:DIS:110019 |
| Corneal Perforation A puncture or hole through the CORNEAL STROMA resulting from various diseases or trauma. | Pathologic Condition | Pathology | Base domain | AMW:DIS:100656 |
| Corneal Ulcer Loss of epithelial tissue from the surface of the cornea due to progressive erosion and necrosis of the tissue; usually caused by bacterial, fungal, … | Pathologic Condition | Pathology | Base domain | AMW:DIS:010383 |
| Corneal Wavefront Aberration Asymmetries in the topography and refractive index of the corneal surface that affect visual acuity. | Disorder | Pathology | Base domain | AMW:DIS:110021 |
| Coronary Aneurysm Abnormal balloon- or sac-like dilatation in the wall of CORONARY VESSELS. Most coronary aneurysms are due to CORONARY ATHEROSCLEROSIS, and the rest a… | Vascular Disorder | Pathology | Base domain | AMW:DIS:140156 |
| Coronary Artery Disease Pathological processes of CORONARY ARTERIES that may derive from a congenital abnormality, atherosclerotic, or non-atherosclerotic cause. | Disorder | Pathology | Base domain | AMW:DIS:140157 |