| AADH | alopecia-anosmia-deafness-hypogonadism [syndrome] |
|---|---|
| ADR | activation, depression, repetition [in bone remodeling]; adrenodoxin reductase; Adriamycin; adverse ... |
| ALDS | albinism-deafness syndrome |
| AVN | acute vasomotor nephropathy; atrioventricular nodal [conduction]; atrioventricular node; avascular n... |
| BADS | black locks-albinism-deafness syndrome |
acute angle
| nerve deafness | Neural deafness, former terms for sensorineural deafness. (05 Mar 2000) |
|---|---|
| noise-induced deafness | A type of sensorineural deafness caused by prolonged exposure to loud sounds, e.g., jet engines. (05 Mar 2000) |
| deafness | A condition in which the sense of hearing in both ears is not functional for ordinary purposes of life. The hearing level for speech is approximately 71 decibels I.s.o. (international organization for standardization) or 61 db a.s.a. (american standards association) or greater. (12 Dec 1998) |
| deafness, sudden | Sensorineural hearing loss which develops over a period of hours or a few days, varying in severity from mild to total. (12 Dec 1998) |
| industrial deafness | Synonym: acoustic trauma deafness. (05 Mar 2000) |
| occupational deafness | Sensorineural hearing loss due to overexposure to high intensity noise levels. Synonym: boilermaker's deafness, industrial deafness, occupational deafness. (05 Mar 2000) |
| organic deafness | Deafness due to a pathologic process or an organic aetiology, as opposed to psychogenic deafness. (05 Mar 2000) |
| functional deafness | Hearing loss without evidence of organic cause or malingering; often follows severe psychic shock. Synonym: functional deafness, hysterical deafness. (05 Mar 2000) |
| low tone deafness | Inability to hear low notes or frequencies. (05 Mar 2000) |
| Albright's hereditary osteodystrophy | An inherited form of hyperparathyroidism associated with ectopic calcification and ossification and skeletal defects, notably the small fourth metacarpals, but intelligence is normal. There are dominant, recessive and X-linked forms. See: pseudohypoparathyroidism. Synonym: Albright's syndrome. (05 Mar 2000) |
| angioedema, hereditary | A genetic form of angioedema. (Angioedema is also referred to as Quinke's disease.) Persons with it are born lacking an inhibitor protein (called C1 esterase inhibitor) that normally prevents activation of a cascade of proteins leading to the swelling of angioedema. Patients can develop recurrent attacks of swollen tissues, pain in the abdomen, and swelling of the voice box (larynx) which can compromise breathing. The diagnosis is suspected with a history of recurrent angioedema. It is confirmed by finding abnormally low levels of C1 esterase inhibitor in the blood. Treatment options include antihistamines and male steroids (androgens) that can also prevent the recurrent attacks. Also called hereditary angioneurotic oedema. (12 Dec 1998) |
| angioneurotic oedema, hereditary | A genetic form of angioedema. (Angioedema is also referred to as Quinke's disease.) Persons with it are born lacking an inhibitor protein (called C1 esterase inhibitor) that normally prevents activation of a cascade of proteins leading to the swelling of angioedema. Patients can develop recurrent attacks of swollen tissues, pain in the abdomen, and swelling of the voice box (larynx) which can compromise breathing. The diagnosis is suspected with a history of recurrent angioedema. It is confirmed by finding abnormally low levels of C1 esterase inhibitor in the blood. Treatment options include antihistamines and male steroids (androgens) that can also prevent the recurrent attacks. Also called hereditary angioedema. (12 Dec 1998) |
| canine hereditary blindness | An autosomal dominant condition seen in dogs of the collie and several other breeds. (05 Mar 2000) |
| colourectal neoplasms, hereditary nonpolyposis | A syndrome characterised by autosomal dominant inheritance, a low mean age (41 years) for occurrence of colon cancer, and a marked increase in the proportion of tumours in the proximal colon. (12 Dec 1998) |
| corneal dystrophies, hereditary | Bilateral hereditary disorders of the cornea, usually autosomal dominant, which may be present at birth but more frequently develop during adolescence and progress slowly throughout life. Central macular dystrophy is transmitted as an autosomal recessive defect. (12 Dec 1998) |