All terms in MESHD
| Label | Id | Description |
|---|---|---|
| Lathyrism | D007842 | [A paralytic condition of the legs caused by ingestion of lathyrogens, especially BETA-AMINOPROPIONITRILE or beta-N-oxalyl amino-L-alanine, which are found in the seeds of plants of the genus LATHYRUS.] |
| Tracheoesophageal Fistula | D014138 | [Abnormal passage between the ESOPHAGUS and the TRACHEA, acquired or congenital, often associated with ESOPHAGEAL ATRESIA.] |
| Respiratory Tract Fistula | D016156 | [An abnormal passage communicating between any component of the respiratory tract or between any part of the respiratory system and surrounding organs.] |
| Tracheal Diseases | D014133 | [Diseases involving the TRACHEA.] |
| Laurence-Moon Syndrome | D007849 | [An autosomal recessive condition characterized by hypogonadism; spinocerebellar degeneration; MENTAL RETARDATION; RETINITIS PIGMENTOSA; and OBESITY. This syndrome was previously referred to as Laurence-Moon-Biedl syndrome until BARDET-BIEDL SYNDROME was identified as a distinct entity. (From N Engl J Med. 1989 Oct 12;321(15):1002-9)] |
| Tracheobronchomegaly | D014137 | [A rare and probably congenital condition characterized by great enlargement of the lumen of the trachea and the larger bronchi.] |
| Bronchial Diseases | D001982 | [Diseases involving the BRONCHI.] |
| Tracheitis | D014136 | [INFLAMMATION of the TRACHEA that is usually associated with RESPIRATORY TRACT INFECTIONS.] |
| Neuroschistosomiasis | D020818 | [SCHISTOSOMIASIS of the brain, spinal cord, or meninges caused by infections with trematodes of the genus SCHISTOSOMA (primarily SCHISTOSOMA JAPONICUM; SCHISTOSOMA MANSONI; and SCHISTOSOMA HAEMATOBIUM in humans). S. japonicum infections of the nervous system may cause an acute meningoencephalitis or a chronic encephalopathy. S. mansoni and S. haematobium nervous system infections are associated with acute transverse myelitis involving the lower portions of the spinal cord. (From Joynt, Clinical Neurology, 1998, Ch27, pp61-2)] |
| Tracheal Stenosis | D014135 | [A pathological narrowing of the TRACHEA.] |
| Tracheal Neoplasms | D014134 | [New abnormal growth of tissue in the TRACHEA.] |
| Hepatitis, Alcoholic | D006519 | [INFLAMMATION of the LIVER due to ALCOHOL ABUSE. It is characterized by NECROSIS of HEPATOCYTES, infiltration by NEUTROPHILS, and deposit of MALLORY BODIES. Depending on its severity, the inflammatory lesion may be reversible or progress to LIVER CIRRHOSIS.] |
| Liver Diseases, Alcoholic | D008108 | [Liver diseases associated with ALCOHOLISM. It usually refers to the coexistence of two or more subentities, i.e., ALCOHOLIC FATTY LIVER; ALCOHOLIC HEPATITIS; and ALCOHOLIC CIRRHOSIS.] |
| Meningitis, Escherichia coli | D020814 | [A form of gram-negative meningitis that tends to occur in neonates, in association with anatomical abnormalities (which feature communication between the meninges and cutaneous structures) or as OPPORTUNISTIC INFECTIONS in association with IMMUNOLOGIC DEFICIENCY SYNDROMES. In premature neonates the clinical presentation may be limited to ANOREXIA; VOMITING; lethargy; or respiratory distress. Full-term infants may have as additional features FEVER; SEIZURES; and bulging of the anterior fontanelle. (From Menkes, Textbook of Child Neurology, 5th ed, pp398-400)] |
| Leukemia, Basophilic, Acute | D015471 | [A rare acute myeloid leukemia in which the primary differentiation is to BASOPHILS. It is characterized by an extreme increase of immature basophilic granulated cells in the bone marrow and blood. Mature basophils are usually sparse.] |
| Leukemia, Prolymphocytic, T-Cell | D015461 | [A lymphoid leukemia characterized by a profound LYMPHOCYTOSIS with or without LYMPHADENOPATHY, hepatosplenomegaly, frequently rapid progression, and short survival. It was formerly called T-cell chronic lymphocytic leukemia.] |
| Leukemia, Prolymphocytic | D015463 | [A chronic leukemia characterized by a large number of circulating prolymphocytes. It can arise spontaneously or as a consequence of transformation of CHRONIC LYMPHOCYTIC LEUKEMIA.] |
| Leukemia, Myeloid, Accelerated Phase | D015465 | [The phase of chronic myeloid leukemia following the chronic phase (LEUKEMIA, MYELOID, CHRONIC-PHASE), where there are increased systemic symptoms, worsening cytopenias, and refractory LEUKOCYTOSIS.] |
| Leukemia, Myeloid, Chronic-Phase | D015466 | [The initial phase of chronic myeloid leukemia consisting of an relatively indolent period lasting from 4 to 7 years. Patients range from asymptomatic to those exhibiting ANEMIA; SPLENOMEGALY; and increased cell turnover. There are 5% or fewer blast cells in the blood and bone marrow in this phase.] |
| Leukemia, Neutrophilic, Chronic | D015467 | [A rare myeloproliferative disorder that is characterized by a sustained, mature neutrophilic leukocytosis. No monocytosis, EOSINOPHILIA, or basophilia is present, nor is there a PHILADELPHIA CHROMOSOME or bcr-abl fusion gene (GENES, ABL).] |