All individuals in MESHD
| Label | Id | Description |
|---|---|---|
| Malignant Hyperthermia | D008305 | [Rapid and excessive rise of temperature accompanied by muscular rigidity following general anesthesia.] |
| Mallory-Weiss Syndrome | D008309 | [A condition characterized by mucosal tears at the ESOPHAGOGASTRIC JUNCTION, sometimes with HEMATEMESIS. Typically it is caused by forceful bouts of retching or VOMITING.] |
| Malnutrition | D044342 | [An imbalanced nutritional status resulting from insufficient intake of nutrients to meet normal physiological requirement.] |
| Malocclusion | D008310 | [Such malposition and contact of the maxillary and mandibular teeth as to interfere with the highest efficiency during the excursive movements of the jaw that are essential for mastication. (Jablonski, Illustrated Dictionary of Dentistry, 1982)] |
| Malocclusion, Angle Class I | D008311 | [Malocclusion in which the mandible and maxilla are anteroposteriorly normal as reflected by the relationship of the first permanent molar (i.e., in neutroclusion), but in which individual teeth are abnormally related to each other.] |
| Malocclusion, Angle Class II | D008312 | [Malocclusion in which the mandible is posterior to the maxilla as reflected by the relationship of the first permanent molar (distoclusion).] |
| Malocclusion, Angle Class III | D008313 | [Malocclusion in which the mandible is anterior to the maxilla as reflected by the first relationship of the first permanent molar (mesioclusion).] |
| Mammary Analogue Secretory Carcinoma | D000069295 | [A malignant neoplasm of epithelial cells of the SALIVARY GLANDS, with microcystic architecture, low-grade nuclei, and granular vacuolated cytoplasm.] |
| Mammary Neoplasms, Animal | D015674 | [Tumors or cancer of the MAMMARY GLAND in animals (MAMMARY GLANDS, ANIMAL).] |
| Mammary Neoplasms, Experimental | D008325 | [Experimentally induced mammary neoplasms in animals to provide a model for studying human BREAST NEOPLASMS.] |
| Mandibular Diseases | D008336 | [Diseases involving the MANDIBLE.] |
| Mandibular Fractures | D008337 | [Fractures of the lower jaw.] |
| Mandibular Injuries | D008338 | [Injuries to the lower jaw bone.] |
| Mandibular Neoplasms | D008339 | [Tumors or cancer of the MANDIBLE.] |
| Mandibulofacial Dysostosis | D008342 | [A hereditary disorder occurring in two forms: the complete form (Franceschetti's syndrome) is characterized by antimongoloid slant of the palpebral fissures, COLOBOMA of the lower lid, MICROGNATHIA and hypoplasia of the ZYGOMATIC ARCHES, and CONGENITAL MICROTIA. It is transmitted as an autosomal trait. The incomplete form (Treacher Collins syndrome) is characterized by the same anomalies in less pronounced degree. It occurs sporadically, but an autosomal dominant mode of transmission is suspected. (Dorland, 27th ed)] |
| Manganese Poisoning | D020149 | [Manganese poisoning is associated with chronic inhalation of manganese particles by individuals who work with manganese ore. Clinical features include CONFUSION; HALLUCINATIONS; and an extrapyramidal syndrome (PARKINSON DISEASE, SECONDARY) that includes rigidity; DYSTONIA; retropulsion; and TREMOR. (Adams, Principles of Neurology, 6th ed, p1213)] |
| Mannosidase Deficiency Diseases | D044904 | [Diseases caused by the loss of one or more enzymes involved in the hydrolysis of mannoside linkages (MANNOSIDASES). The defects in enzyme activity are primarily associated with genetic mutation of the genes that codes for a particular mannosidase isoenzyme.] |
| Mansonelliasis | D008368 | [Infection with nematodes of the genus MANSONELLA. Symptoms include pruritus, headache, and articular swelling.] |
| Maple Syrup Urine Disease | D008375 | [An autosomal recessive inherited disorder with multiple forms of phenotypic expression, caused by a defect in the oxidative decarboxylation of branched-chain amino acids (AMINO ACIDS, BRANCHED-CHAIN). These metabolites accumulate in body fluids and render a "maple syrup" odor. The disease is divided into classic, intermediate, intermittent, and thiamine responsive subtypes. The classic form presents in the first week of life with ketoacidosis, hypoglycemia, emesis, neonatal seizures, and hypertonia. The intermediate and intermittent forms present in childhood or later with acute episodes of ataxia and vomiting. (From Adams et al., Principles of Neurology, 6th ed, p936)] |
| Marburg Virus Disease | D008379 | [An RNA virus infection of rhesus, vervet, and squirrel monkeys transmissible to man.] |