| HAM | 1) Human Albumin Microsphere 2) HTLV-1 Associated Myelopath... |
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| AIM | Abridged Index Medicus; acute transverse myelopathy; area of interest magnification; artificial inte... |
| ATM | abnormal tubular myelin; acute transverse myelopathy; asynchronous transfer mode; atmosphere |
| PTPM | post-traumatic progressive myelopathy |
| SCM | Schwann cell membrane; sensation, circulation, and motion; Society of Computer Medicine; soluble cyt... |
| ATM | Acute transverse myelopathy |
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| CSM | Cervical spondylotic myelopathy |
| HAM/TSP | HTLV I associated myelopathy/tropical spastic paraparesis |
| HAM | HTLV associated myelopathy |
| TSP/HAM | Tropical Spastic Paraparesis/HTLV-I associated myelopathy |
| carcinomatous myelopathy | Degeneration or necrosis of the spinal cord associated with a carcinoma. Synonym: paracarcinomatous myelopathy. (05 Mar 2000) |
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| radiation myelopathy | Damage to the spinal cord from exposure to X-rays or other high energy radiation; usually radiation myelitis. Synonym: radiation myelitis. (05 Mar 2000) |
| paracarcinomatous myelopathy | Degeneration or necrosis of the spinal cord associated with a carcinoma. Synonym: paracarcinomatous myelopathy. (05 Mar 2000) |
| compressive myelopathy | Destruction of spinal cord tissue caused by pressure from neoplasms, haematomas, or other masses. (05 Mar 2000) |
| myelopathy | <pathology> Any disease affecting the spinal cord. Origin: Gr. Pathos = disease (09 Oct 1997) |
| diabetic myelopathy | <pathology> Degenerative changes in spinal cord tissue occurring as a complication of diabetes mellitus Origin: Gr. Pathos = disease (27 Sep 1997) |
| 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) |
| hereditary | <genetics> Transferred via genes from parent to child. (16 Dec 1997) |
| hereditary amyloidosis | <neurology> A disorder in which various peripheral nerves are infiltrated with amyloid and their functions disturbed, an abnormal prealbumin is also formed and is present in the blood; characteristically, it begins during mid-life and is found largely in persons of Portuguese descent. Other rare clinical types occur. Inheritance: autosomal dominant. Synonym: familial amyloidosis, hereditary amyloidosis. (05 Mar 2000) |
| hereditary angioedema | 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) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|