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 |
|---|---|---|---|---|
| Color Vision Defects Defects of color vision are mainly hereditary traits but can be secondary to acquired or developmental abnormalities in the CONES (RETINA). Severity … | Pathologic Condition | Pathology | Base domain | AMW:DIS:100569 |
| Colorado Tick Fever A febrile illness characterized by chills, aches, vomiting, leukopenia, and sometimes encephalitis. It is caused by the COLORADO TICK FEVER VIRUS, a … | Infectious Disorder | Pathology | Base domain | AMW:DIS:010630 |
| Colorectal Neoplasms Tumors or cancer of the COLON or the RECTUM or both. Risk factors for colorectal cancer include chronic ULCERATIVE COLITIS; FAMILIAL POLYPOSIS COLI; … | Neoplastic Disorder | Pathology | Base domain | AMW:DIS:040509 |
| Colorectal Neoplasms, Hereditary Nonpolyposis A group of autosomal-dominant inherited diseases in which COLON CANCER arises in discrete adenomas. Unlike FAMILIAL POLYPOSIS COLI with hundreds of p… | Neoplastic Disorder | Pathology | Base domain | AMW:DIS:040513 |
| Coma A profound state of unconsciousness associated with depressed cerebral activity from which the individual cannot be aroused. Coma generally occurs wh… | Pathologic Condition | Pathology | Base domain | AMW:DIS:100480 |
| Coma, Post-Head Injury Prolonged unconsciousness from which the individual cannot be aroused, associated with traumatic injuries to the BRAIN. This may be defined as uncons… | Traumatic Disorder | Pathology | Base domain | AMW:DIS:100481 |
| Common Bile Duct Diseases Diseases of the COMMON BILE DUCT including the AMPULLA OF VATER and the SPHINCTER OF ODDI. | Disorder | Pathology | Base domain | AMW:DIS:060014 |
| Common Bile Duct Neoplasms Tumor or cancer of the COMMON BILE DUCT including the AMPULLA OF VATER and the SPHINCTER OF ODDI. | Neoplastic Disorder | Pathology | Base domain | AMW:DIS:040502 |
| Common Cold A catarrhal disorder of the upper respiratory tract, which may be viral or a mixed infection. It generally involves a runny nose, nasal congestion, a… | Infectious Disorder | Pathology | Base domain | AMW:DIS:010555 |
| Common Variable Immunodeficiency Heterogeneous group of immunodeficiency syndromes characterized by hypogammaglobulinemia of most isotypes, variable B-cell defects, and the presence … | Immune Disorder | Pathology | Base domain | 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 | Base domain | AMW:DIS:140064 |
| Communicable Diseases An illness caused by an infectious agent or its toxins that occurs through the direct or indirect transmission of the infectious agent or its product… | Infectious Disorder | Pathology | Base domain | AMW:DIS:010351 |
| Communicable Diseases, Emerging Infectious diseases that are novel in their outbreak ranges (geographic and host) or transmission mode. | Infectious Disorder | Pathology | Base domain | AMW:DIS:010369 |
| Communicable Diseases, Imported Infectious diseases originating in one geographically delineated ecosystem that are carried (by travel or immigration) to another geographically deli… | Infectious Disorder | Pathology | Base domain | AMW:DIS:010370 |
| Community-Acquired Infections Any infection acquired in the community, that is, contrasted with those acquired in a health care facility (CROSS INFECTION). An infection would be c… | Infectious Disorder | Pathology | Base domain | AMW:DIS:010377 |
| Community-Acquired Pneumonia Infection of the lungs in a patient who is not hospitalized or who has not resided in a long-term care facility for 14 days prior to the onset of sym… | Infectious Disorder | Pathology | Base domain | AMW:DIS:010378 |
| 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 | Base domain | AMW:DIS:050243 |
| Compassion Fatigue Emotional distress caused by repeated or prolonged expression of compassion or empathy. It may occur in individuals working in care giving profession… | Pathologic Condition | Pathology | Base domain | AMW:DIS:230249 |
| 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 | Base domain | AMW:DIS:100029 |
| Composite Lymphoma Two or more distinct types of malignant lymphoid tumors occurring within a single organ or tissue at the same time. It may contain different types of… | Neoplastic Disorder | Pathology | Base domain | AMW:DIS:040099 |
| Conducted Energy Weapon Injuries The injuries caused by conducted energy weapons such as stun guns, shock batons, and cattle prods. | Traumatic Disorder | Pathology | Base domain | AMW:DIS:260038 |
| Condylomata Acuminata Sexually transmitted form of anogenital warty growth caused by the HUMAN PAPILLOMAVIRUS VIRUSES. | Infectious Disorder | Pathology | Base domain | AMW:DIS:010375 |
| 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 | Base domain | 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 | Base domain | AMW:DIS:110048 |
| Congenital Abnormalities Malformations of organs or body parts during development in utero. | Congenital Disorder | Pathology | Base domain | AMW:DIS:160002 |
| 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 | Base domain | 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 | Base domain | AMW:DIS:100354 |
| Congenital Disorders of Glycosylation A genetically heterogeneous group of heritable disorders resulting from defects in protein N-glycosylation. | Congenital Disorder | Pathology | Base domain | AMW:DIS:160083 |
| Congenital Hyperinsulinism A familial, nontransient HYPOGLYCEMIA with defects in negative feedback of GLUCOSE-regulated INSULIN release. Clinical phenotypes include HYPOGLYCEMI… | Congenital Disorder | Pathology | Base domain | 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 | Base domain | AMW:DIS:050010 |