| MEA | male-enhanced antigen; Medical Exhibition Association; mercaptoethylamine; monoethanolamine; multipl... |
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| M/F | male/female [ratio] |
| M& | F male and female; mother and father |
| MIT | Massachusetts Institute of Technology; male impotence test; marrow iron turnover; melodic intonation... |
| MPB | male pattern baldness; meprobamate |
| internal male genital organs | The internal masculine genital organs, the testes, epididymides, deferent ducts, seminal vesicles, prostate, and bulbourethral glands. Synonym: organa genitalia masculina interna. (05 Mar 2000) |
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| iodide transport defect | See: familial goiter. (05 Mar 2000) |
| iodotyrosine deiodinase defect | See: familial goiter. (05 Mar 2000) |
| oesophageal filling defect | <radiology> Tumour, carcinoma (oesophagus, stomach extending proximally), leiomyoma / leiomyosarcoma, polyp: fibrovascular, inflammatory, adenomatous, papilloma, carcinosarcoma, lymphoma, metastasis, oesophageal varix, extrinsic lesion (vascular impression, adenopathy, cyst), foreign body (12 Dec 1998) |
| osteoporotic marrow defect | Focal osteoporotic bone marrow defect of the jaw; a focal radiolucent defect composed of normal marrow. (05 Mar 2000) |
| Eisenmenger's defect | The combination of ventricular septal defect with pulmonary hypertension and consequent right-to-left shunt through the defect, with or without an associated overriding aorta. Synonym: Eisenmenger's defect, Eisenmenger's disease, Eisenmenger's tetralogy. (05 Mar 2000) |
| endocardial cushion defect | <radiology> Persistence of primitive atrioventricular canal and anomalies of AV valves associated with: Down syndrome: in 25% of Trisomy 21 an ECD is present; in 45% of ECD Trisomy 21 is present, asplenia/polysplenia types: complete (AV canal), partial findings: gooseneck deformity on angiogram, increased pulmonary vascularity, enlarged pulmonary artery, enlarged RV, LV, RA; normal LA (secondary to atrial septal defect) (12 Dec 1998) |
| enzyme defect | A disorder resulting from a deficiency (or functional abnormality) of an enzyme. In 1902 Archibald Garrod first attributed a disease to an enzyme defect: an inborn error of metabolism. Today, newborns are routinely screened for certain enzyme defects such as PKU (phenylketonuria) and galactosaemia, an error in the handling (metabolism) of the sugar galactose. (12 Dec 1998) |
| tuberculosis, male genital | Tuberculosis of the genitalia in men. (12 Dec 1998) |
| external male genital organs | The external masculine genital organs, the penis and scrotum. Synonym: organa genitalia masculina externa. (05 Mar 2000) |
| fertility agents, male | Compounds which increase the capacity of the male to induce conception. (12 Dec 1998) |
| urethral crest of male | A longitudinal fold on the posterior wall of the urethra extending from the uvula of the bladder through the prostatic urethra; prominent in its midportion is the seminal colliculus. Synonym: crista phallica, crista urethralis masculinae. (05 Mar 2000) |
| fibrous cortical defect | A common 1 to 3 cm defect in the cortex of a bone, most commonly the lower femoral shaft of a child, filled with fibrous tissue. Nonosteogenic or nonossifying fibroma by convention refers to lesions greater than 3 cm in diameter. See: nonossifying fibroma. Synonym: nonosteogenic fibroma. (05 Mar 2000) |
| urologic and male genital diseases | A collective term for urinary tract diseases in male and female and diseases of the male genitalia. (12 Dec 1998) |
| urologic surgical procedures, male | Surgery performed on the male genitalia. (12 Dec 1998) |