| hereditary deafness and nephropathy | <nephrology, pathology> An inherited disorder involving damage to the kidneys, haematuria and hearing loss. In some individuals vision may also be affected. This genetic disease is uncommon. Symptoms include loss of hearing, abnormal colour to urine, swelling, cough and decline in vision. Inheritance: sex-linked autosomal dominant. Incidence: 1 in 50,000. Origin: Gr. Pathos = disease (27 Sep 1997) |
|---|---|
| hereditary deforming chondrodystrophy | A disturbance of enchondral bone growth in which multiple, generally benign osteochondromas of long bones appear during childhood, commonly with shortening of the radius and fibula; the ill-effects are usually mechanical but malignant change is rare; autosomal dominant inheritance. Synonym: diaphysial aclasis, hereditary deforming chondrodystrophy, multiple exostosis, osteochondromatosis. (05 Mar 2000) |
| hereditary exostosis | <radiology> (osteochondromatosis) Autosomal dominant, M more than F, multiple exostoses, snowflake calcification of mature cartilage cap, may leading to chondrosarcoma, short metacarpals (especially 4th and 5th) (12 Dec 1998) |
| hereditary fructose intolerance | A metabolic error due to deficiency of hepatic fructose 1,6-bisphosphate aldolase B (which also acts on fructose 1-phosphate); the second enzyme in the specific fructose pathway; vomiting and hypoglycaemia follow ingestion of fructose; prolonged fructose ingestion in young children results in failure to thrive and in jaundice, hepatomegaly, albuminuria, aminoaciduria, and sometimes cachexia and death; autosomal recessive inheritance in most families. (05 Mar 2000) |
| hereditary haemorrhagic telangiectasia | <gastroenterology> An inherited disease characterised by thin blood vessel walls in the nose, skin and gastrointestinal tract. This condition ins associated with a high risk of bleeding complications. Inheritance: autosomal dominant. (27 Sep 1997) |
| hereditary haemorrhagic thrombasthenia | <haematology> A form of congenital platelet functional defect that result in prolongation of the bleeding time. Characteristics include mucosal and post-operative bleeding that may be severe. (17 Dec 1997) |
| hereditary hyperthyroidism | A rare inherited (autosomal dominant) disorder with constitutive stimulation of the thyrocytes. (05 Mar 2000) |
| hereditary hypertrophic neuropathy | dejerine-Sottas disease |
| hereditary lymphedema | Permanent pitting oedema usually confined to the legs; two types, congenital (Milroy's disease ), or with onset at about the age of puberty (Meige's disease ); autosomal dominant inheritance. (05 Mar 2000) |
| hereditary methemoglobinaemia | Methemoglobinaemia due to formation of any one of a group of abnormal a chain or b chain haemoglobins collectively known as haemoglobin M. Slate-gray cyanosis occurs in early infancy, without pulmonary or cardiac disease, and is resistant to ascorbic acid or methylene blue therapy; autosomal dominant inheritance, methemoglobinaemia due to deficiency of cytochrome b5 reductaseor methemoglobin reductase, the enzyme responsible for reduction of intraerythrocyte methemoglobin; cyanosis is improved by ascorbic acid or methylene blue; autosomal recessive inheritance, one case of methemoglobinaemia has been reported that apparently is due to a deficiency of cytochrome b5. Synonym: hereditary methemoglobinaemia, hereditary methemoglobinaemic cyanosis, primary methemoglobinaemia. (05 Mar 2000) |
| hereditary methemoglobinaemic cyanosis | Methemoglobinaemia due to formation of any one of a group of abnormal a chain or b chain haemoglobins collectively known as haemoglobin M. Slate-gray cyanosis occurs in early infancy, without pulmonary or cardiac disease, and is resistant to ascorbic acid or methylene blue therapy; autosomal dominant inheritance, methemoglobinaemia due to deficiency of cytochrome b5 reductaseor methemoglobin reductase, the enzyme responsible for reduction of intraerythrocyte methemoglobin; cyanosis is improved by ascorbic acid or methylene blue; autosomal recessive inheritance, one case of methemoglobinaemia has been reported that apparently is due to a deficiency of cytochrome b5. Synonym: hereditary methemoglobinaemia, hereditary methemoglobinaemic cyanosis, primary methemoglobinaemia. (05 Mar 2000) |
| hereditary multiple exostoses | A disturbance of enchondral bone growth in which multiple, generally benign osteochondromas of long bones appear during childhood, commonly with shortening of the radius and fibula; the ill-effects are usually mechanical but malignant change is rare; autosomal dominant inheritance. Synonym: diaphysial aclasis, hereditary deforming chondrodystrophy, multiple exostosis, osteochondromatosis. (05 Mar 2000) |
| hereditary multiple trichoepithelioma | <tumour> Multiple small benign nodules, occurring mostly on the skin of the face, derived from basal cells of hair follicles enclosing small keratin cysts; frequent autosomal dominant inheritance. Synonym: acanthoma adenoides cysticum, Brooke's tumour, epithelioma adenoides cysticum, hereditary multiple trichoepithelioma. Origin: tricho-+ epithelioma (05 Mar 2000) |
| hereditary mutation | A gene change that occurs in a germ cell (an egg or sperm) to become incorporated in every cell in the body. Hereditary mutations (also called germline mutations) play a role in cancer as, for example, the eye tumour retinoblastoma and wilms' tumour of the kidney. (12 Dec 1998) |
| hereditary myokymia | A syndrome consisting of myokymia, hypoglycaemia, and disturbed thyroid function. (05 Mar 2000) |
Synonyms : Hernandia
Synonyms : Hernias
Synonyms : Abdominal Hernia, Abdominal Hernias, Hernias, Abdominal
Synonyms : Diaphragmatic Hernias, Hernias, Diaphragmatic
Synonyms : Diaphragmatic Hernias, Traumatic, Hernia, Traumatic Diaphragmatic, Hernias, Traumatic Diaphragmatic, Traumatic Diaphragmatic Hernia, Traumatic Diaphragmatic Hernias
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|---|---|---|---|
|
헤라코프시럽 - 새창
|
동화약품공업 |
A05752871 | Hederae helix fluid | 일반의약품 | 급여 |
|
헤라콜시럽 - 새창
|
삼천당제약 |
A08451671 | Hederae helix fluid | 일반의약품 | 급여 |
|
헤라스판시럽 - 새창
|
유한메디카 |
A42950461 | Hederae helix fluid | 일반의약품 | 급여 |
|
헤로틴정 - 새창
|
동광제약 |
A01352741 | Carbonyl iron | 일반의약품 | 삭제 |
|
허셉틴주150mg - 새창
|
F.Hoffmann-La Roche |
E01840761 | Trastuzumab | 전문의약품 | 급여 |
|
헤르벤정 - 새창
|
한일약품공업 |
A01001991 | Diltiazem HCl | 전문의약품 | 삭제 |
|
헤로틴정45mg - 새창
|
동광제약 |
A01306801 | Carbonyl iron | 일반의약품 | 급여 |
|
헤르벤서방정90mg - 새창
|
씨제이 |
A11602320 | Diltiazem HCl | 전문의약품 | 급여 |
|
헤르벤서방캅셀180mg - 새창
|
씨제이 |
A11650641 | Diltiazem HCl | 전문의약품 | 급여 |
|
헤르벤주50mg - 새창
|
씨제이 |
A11602681 | Diltiazem HCl | 전문의약품 | 급여 |
| herb |
a plant lacking a permanent woody stem; many are flowering garden plants or potherbs; some having medicinal properties; some are pests aromatic potherb used in cookery for its savory qualities
출처: wordnet.princeton.edu/perl/webwn
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|---|---|
| hertz |
the unit of frequency; one hertz has a periodic interval of one second German physicist who was the first to produce electromagnetic waves artificially (1857-1894) German physicist who with James Franck proved the existence of the stationary energy states postulated by Bohr (1887-1975)
출처: wordnet.princeton.edu/perl/webwn
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| herb tea |
tea-like drink made of leaves of various herbs
출처: wordnet.princeton.edu/perl/webwn
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| herbalist |
a therapist who heals by the use of herbs
출처: wordnet.princeton.edu/perl/webwn
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| hereditary motor and sensory neuropathy |
Charcot-Marie-Tooth disease: a form of neuropathy that can begin between childhood and young adulthood; characterized by weakness and atrophy of the muscles of the hands and lower legs; progression is slow and individuals affected can have a normal life span; inheritance is X-linked recessive or X-linked dominant
출처: wordnet.princeton.edu/perl/webwn
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| HER | tea-like drink made of leaves of various herbs |
|---|---|
| HER | the use of plants or plant extracts for medicinal purposes (especially plants that are not part of the normal diet) |
| HER | a therapist who heals by the use of herbs |
| HER | German philosopher (1776-1841) |
| HER | United States musician and composer and conductor noted for his comic operas (1859-1924) |
| HER | United States economist and psychologist who pioneered in the development of cognitive science (1916-2001) |
| HER | United States economist and psychologist who pioneered in the development of cognitive science (1916-2001) |
| HER | United States actor |
| HER | 31st President of the United States |
| HER | prolific English writer best known for his science-fiction novels |
| HER | 31st President of the United States |
| HER | British field marshal (1850-1916) |