| IP | icterus praecox; imaging plate; immune precipitate; immunoblastic plasma; immunoperoxidase technique... |
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| IPA | immunoperoxidase assay; incontinentia pigmenti achromians; independent physician or practice associa... |
| IP | Incontinentia Pigmenti |
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| ectasia ventriculi paradoxa | A condition in which there is a central constriction of the wall of the stomach dividing it into two cavities, cardiac and pyloric. Synonym: bilocular stomach, ectasia ventriculi paradoxa. Leather-bottle stomach, marked thickening and rigidity of the stomach wall, with reduced capacity of the lumen although often without obstruction; nearly always due to scirrhous carcinoma, as in linitis plastica. Synonym: sclerotic stomach. (05 Mar 2000) |
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| syndrome, incontinentia pigmenti | A genetic disease with blisters that develop soon after birth on the trunk and limbs, then heal, but leave dark (hyperpigmented) streaks and marble-like whorls on the skin. (the name came from the erroneous idea that the skin cells were incontinent of pigment and could not contain it normally.) other key features of ip include dental and nail abnormalities, bald patches, and (in about 1/3rd of cases) mental retardation. Ip is an x-linked dominant with male lethality. The ip gene is in band q28 on the x chromosome. Mothers with ip have an equal chance of having a normal or ip daughter or a normal son. The ip sons die before birth. Ip is also known as bloch-sulzberger syndrome. (12 Dec 1998) |
| incontinentia | <gastroenterology, urology> The inability to control excretory functions, as defecation (faecal incontinence) or urination (urinary incontinence). Origin: L. Incontinentia (13 Nov 1997) |
| incontinentia pigmenti | A genetic disease with blisters that develop soon after birth on the trunk and limbs, then heal, but leave dark (hyperpigmented) streaks and marble-like whorls on the skin. (the name came from the erroneous idea that the skin cells were incontinent of pigment and could not contain it normally.) other key features of ip include dental and nail abnormalities, bald patches, and (in about 1/3rd of cases) mental retardation. Ip is an x-linked dominant with male lethality. The ip gene is in band q28 on the x chromosome. Mothers with ip have an equal chance of having a normal or ip daughter or a normal son. The ip sons die before birth. Ip is also known as bloch-sulzberger syndrome. (12 Dec 1998) |
| incontinentia pigmenti achromians | Inherited hypopigmented macules in a "marble-cake" pattern, variably associated with epidermal nevi, alopecia, and ocular, skeletal, and neural abnormalities. Synonym: hypomelanosis of Ito. (05 Mar 2000) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|