All terms in MESHD
| Label | Id | Description |
|---|---|---|
| Cyanosis | D003490 | [A bluish or purplish discoloration of the skin and mucous membranes due to an increase in the amount of deoxygenated hemoglobin in the blood or a structural defect in the hemoglobin molecule.] |
| Hepatitis, Animal | D006520 | [INFLAMMATION of the LIVER in non-human animals.] |
| Hepatitis, Chronic | D006521 | [An aggressive form of chronic hepatitis involving extensive liver damage and cell injury beyond the portal tract., A mild form of chronic hepatitis causing limited damage to the liver., INFLAMMATION of the LIVER with ongoing hepatocellular injury for 6 months or more, characterized by NECROSIS of HEPATOCYTES and inflammatory cell (LEUKOCYTES) infiltration. Chronic hepatitis can be caused by viruses, medications, autoimmune diseases, and other unknown factors.] |
| Hepatitis, Viral, Animal | D006524 | [INFLAMMATION of the LIVER in animals due to viral infection.] |
| Lead Poisoning | D007855 | [Poisoning that results from chronic or acute ingestion, injection, inhalation, or skin absorption of LEAD or lead compounds.] |
| Hepatitis, Infectious Canine | D006522 | [A contagious disease caused by canine adenovirus (ADENOVIRUSES, CANINE) infecting the LIVER, the EYE, the KIDNEY, and other organs in dogs, other canids, and bears. Symptoms include FEVER; EDEMA; VOMITING; and DIARRHEA.] |
| Adenoviridae Infections | D000257 | [Virus diseases caused by the ADENOVIRIDAE.] |
| Campylobacter Infections | D002169 | [Infections with bacteria of the genus CAMPYLOBACTER.] |
| Carcinoma, Hepatocellular | D006528 | [A primary malignant neoplasm of epithelial liver cells. It ranges from a well-differentiated tumor with EPITHELIAL CELLS indistinguishable from normal HEPATOCYTES to a poorly differentiated neoplasm. The cells may be uniform or markedly pleomorphic, or form GIANT CELLS. Several classification schemes have been suggested.] |
| Liver Neoplasms | D008113 | [Tumors or cancer of the LIVER.] |
| Learning Disorders | D007859 | [Conditions characterized by a significant discrepancy between an individual's perceived level of intellect and their ability to acquire new language and other cognitive skills. These disorders may result from organic or psychological conditions. Relatively common subtypes include DYSLEXIA, DYSCALCULIA, and DYSGRAPHIA.] |
| Hepatomegaly | D006529 | [Enlargement of the liver.] |
| Hypertrophy | D006984 | [General increase in bulk of a part or organ due to CELL ENLARGEMENT and accumulation of FLUIDS AND SECRETIONS, not due to tumor formation, nor to an increase in the number of cells (HYPERPLASIA).] |
| Pseudobulbar Palsy | D020828 | [A syndrome characterized by DYSARTHRIA, dysphagia, dysphonia, impairment of voluntary movements of tongue and facial muscles, and emotional lability. This condition is caused by diseases that affect the motor fibers that travel from the cerebral cortex to the lower BRAIN STEM (i.e., corticobulbar tracts); including MULTIPLE SCLEROSIS; MOTOR NEURON DISEASE; and CEREBROVASCULAR DISORDERS. (From Adams et al., Principles of Neurology, 6th ed, p489)] |
| Paralysis | D010243 | [A general term most often used to describe severe or complete loss of muscle strength due to motor system disease from the level of the cerebral cortex to the muscle fiber. This term may also occasionally refer to a loss of sensory function. (From Adams et al., Principles of Neurology, 6th ed, p45)] |
| Hepatitis C | D006526 | [INFLAMMATION of the LIVER in humans caused by HEPATITIS C VIRUS, a single-stranded RNA virus. Its incubation period is 30-90 days. Hepatitis C is transmitted primarily by contaminated blood parenterally, and is often associated with transfusion and intravenous drug abuse. However, in a significant number of cases, the source of hepatitis C infection is unknown.] |
| Flaviviridae Infections | D018178 | [Infections with viruses of the family FLAVIVIRIDAE.] |
| Hepatolenticular Degeneration | D006527 | [A rare autosomal recessive disease characterized by the deposition of copper in the BRAIN; LIVER; CORNEA; and other organs. It is caused by defects in the ATP7B gene encoding copper-transporting ATPase 2 (EC 3.6.3.4), also known as the Wilson disease protein. The overload of copper inevitably leads to progressive liver and neurological dysfunction such as LIVER CIRRHOSIS; TREMOR; ATAXIA and intellectual deterioration. Hepatic dysfunction may precede neurologic dysfunction by several years.] |
| Movement Disorders | D009069 | [Syndromes which feature DYSKINESIAS as a cardinal manifestation of the disease process. Included in this category are degenerative, hereditary, post-infectious, medication-induced, post-inflammatory, and post-traumatic conditions.] |
| Trachoma | D014141 | [A chronic infection of the CONJUNCTIVA and CORNEA caused by CHLAMYDIA TRACHOMATIS.] |