All terms in MESHD
| Label | Id | Description |
|---|---|---|
| Pneumonia, Aspiration | D011015 | [A type of lung inflammation resulting from the aspiration of food, liquid, or gastric contents into the upper RESPIRATORY TRACT.] |
| Aicardi Syndrome | D058540 | [A rare genetic disorder characterized by partial or complete absence of the CORPUS CALLOSUM, resulting in infantile spasms, MENTAL RETARDATION, and lesions of the RETINA or OPTIC NERVE.] |
| Pectus Carinatum | D066166 | [A developmental anomaly characterized by abnormal anterior protrusion of the STERNUM and adjacent COSTAL CARTILAGE.] |
| Still's Disease, Adult-Onset | D016706 | [Systemic-onset rheumatoid arthritis in adults. It differs from classical rheumatoid arthritis in that it is more often marked by acute febrile onset, and generalized lymphadenopathy and hepatosplenomegaly are more prominent.] |
| Pneumoperitoneum | D011027 | [A condition with trapped gas or air in the PERITONEAL CAVITY, usually secondary to perforation of the internal organs such as the LUNG and the GASTROINTESTINAL TRACT, or to recent surgery. Pneumoperitoneum may be purposely introduced to aid radiological examination.] |
| Pneumopericardium | D011026 | [Presence of air or gas in the space between the heart and the PERICARDIUM. The degree of respiratory distress depends on the amount of trapped air and circulation blocked in the systemic and pulmonary veins.] |
| Pneumonia, Staphylococcal | D011023 | [Pneumonia caused by infections with bacteria of the genus STAPHYLOCOCCUS, usually with STAPHYLOCOCCUS AUREUS.] |
| Staphylococcal Infections | D013203 | [Infections with bacteria of the genus STAPHYLOCOCCUS.] |
| Pneumonia, Viral | D011024 | [Inflammation of the lung parenchyma that is caused by a viral infection.] |
| Telangiectasis | D013684 | [Permanent dilation of preexisting blood vessels (CAPILLARIES; ARTERIOLES; VENULES) creating small focal red lesions, most commonly in the skin or mucous membranes. It is characterized by the prominence of skin blood vessels, such as vascular spiders.] |
| Pneumonia, Progressive Interstitial, of Sheep | D011021 | [Chronic respiratory disease caused by the VISNA-MAEDI VIRUS. It was formerly believed to be identical with jaagsiekte (PULMONARY ADENOMATOSIS, OVINE) but is now recognized as a separate entity.] |
| Pneumonia, Rickettsial | D011022 | [Pneumonia caused by infection with bacteria of the family RICKETTSIACEAE.] |
| Rickettsiaceae Infections | D012288 | [Infections with bacteria of the family RICKETTSIACEAE.] |
| Telangiectasia, Hereditary Hemorrhagic | D013683 | [An autosomal dominant vascular anomaly characterized by telangiectases of the skin and mucous membranes and by recurrent gastrointestinal bleeding. This disorder is caused by mutations of a gene (on chromosome 9q3) which encodes endoglin, a membrane glycoprotein that binds TRANSFORMING GROWTH FACTOR BETA.] |
| Pneumonia, Pneumocystis | D011020 | [A pulmonary disease in humans occurring in immunodeficient or malnourished patients or infants, characterized by DYSPNEA, tachypnea, and HYPOXEMIA. Pneumocystis pneumonia is a frequently seen opportunistic infection in AIDS. It is caused by the fungus PNEUMOCYSTIS JIROVECII. The disease is also found in other MAMMALS where it is caused by related species of Pneumocystis.] |
| Pneumocystis Infections | D016720 | [Infections with species in the genus PNEUMOCYSTIS, a fungus causing interstitial plasma cell pneumonia (PNEUMONIA, PNEUMOCYSTIS) and other infections in humans and other MAMMALS. Immunocompromised patients, especially those with AIDS, are particularly susceptible to these infections. Extrapulmonary sites are rare but seen occasionally.] |
| Congenital Hypothyroidism | D003409 | [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, such as thyroid dysgenesis or HYPOTHYROIDISM in infants of mothers treated with THIOURACIL during pregnancy. Endemic cretinism is the result of iodine deficiency. Clinical symptoms include severe MENTAL RETARDATION, impaired skeletal development, short stature, and MYXEDEMA.] |
| Post-Lyme Disease Syndrome | D000077342 | [A subjective syndrome that occurs following standard antibiotic treatment of Lyme disease. It includes FATIGUE; MUSCULOSKELETAL PAIN; and neurocognitive dysfunction., A condition caused by long-lasting and ongoing infection with the spirochete Borrelia burgdorferi resulting in progressive inflammatory neurologic, neuromuscular, and dermatologic manifestations including ENCEPHALITIS; MYELITIS; acrodermatitis chronica atrophicans; and ARTHRITIS.] |
| Yin Deficiency | D016710 | [In the YIN-YANG system of philosophy and medicine, an insufficiency of body fluid (called yinxu), manifesting often as irritability, thirst, constipation, etc. (The Pinyin Chinese-English Dictionary, 1979).] |
| Yang Deficiency | D016711 | [In the YIN-YANG system of philosophy and medicine, a lack of vital energy (called yangxu in Chinese). It manifests itself in various systemic and organic diseases. (The Pinyin Chinese-English Dictionary, 1979)] |