| IED | inherited epidermal dysplasia; intermittent explosive disorder |
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| MIDD | Maternally Inherited Diabetes and Deafness |
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| parakeratosis | <pathology> Persistence of the nuclei in the cells of the stratum corneum of the epidermis, as seen, for example: in psoriasis. (09 Oct 1997) |
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| parakeratosis ostracea | parakeratosis scutularis |
| parakeratosis variegata | A rare condition that simulates chronic radiodermatitis in appearance; may eventuate as mycosis fungoides. Synonym: parakeratosis variegata, parapsoriasis lichenoides. Poikiloderma of Civatte, reticulated pigmentation and telangiectasia of the sides of the cheeks and neck; common in middle-aged women. Synonym: Civatte's disease. (05 Mar 2000) |
| porcine parakeratosis | A skin disease of young pigs characterised by a hard, scaly proliferation of the surface layers of the skin. The extremities are commonly affected first, but it may involve the entire body. Parakeratosis psoriasiformis, an eruption marked by the presence of thick scales resembling those of psoriasis. Parakeratosis pustulosa, idiopathic subungual keratosis with nail deformity or pitting and with pustular or well-demarcated scaling eczematous changes of the fingertips; usually seen in young girls. Parakeratosis scutularis, a disease of the scalp marked by the formation of crusts that envelop the hairs. Synonym: parakeratosis ostracea. (05 Mar 2000) |
| dominantly inherited Levi's disease | Dwarfism characterised by low birth weight, snub nose, and stocky build; autosomal dominant inheritance. There is a similar autosomal recessive phenotype. Synonym: dominantly inherited Levi's disease. (05 Mar 2000) |
| inherited | Derived from a preformed genetic code present in the parents. Contrast with acquired. (05 Mar 2000) |
| inherited albumin variants | Types of human serum albumin, distinguished by characteristic mobility patterns on electrophoresis; each type is due to a mutation of a gene controlling albumin synthesis; the mutant genes are codominant with the normal gene for albumin A, and the group forms a system of genetic polymorphism; types include: albumin b (slow), found occasionally in persons of European ancestry; albumin Ghent (fast), found first at Ghent, Belgium; albumin Mexico (slow), found in Indians of Mexico and the southwestern United States; albumin Naskapi (fast), found in the Naskapi and other Indians of northern North America; and albumin Reading (fast), found first at Reading, England. (05 Mar 2000) |
| inherited character | A single attribute of an animal or plant that is transmitted at one locus from generation to generation in accordance with Mendel's law. See: gene. Synonym: unit character. (05 Mar 2000) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|