| 영문 | teeth | 한글 | 치아, 이빨 |
|---|---|---|---|
| 설명 | 위턱과 아래턱의 이틀돌기 내에 위치하는 단단한 석회화된 구조로서 음식물을 씹는데 사용됨. 사람에게는 생후 2년반에 나오는 모두 20개가 되는 유 나오는 모두 20개가 되는 젖니와 젖니가 빠진 후 나오는 모두 32개가 되는 영구치의 두 종류의 치아가 존재한다. 치아는 모양에 따라 앞니(incisor), 송곳니(canine), 어금니(molar)의 세 종류가 있다. |
||
| DEF | decayed primary teeth requiring filling, decayed primary teeth requiring extraction, and primary tee... |
|---|---|
| DM-R | decayed plus missing teeth, minus replaced teeth |
| NAT | N-acetyltransferase; natal; neonatal alloimmune thrombocytopenia; no action taken; nonaccidental tra... |
| DMF | decayed, missing, and filled [teeth]; N,N-dimethylformamide; diphasic milk fever |
| REEDS | retention of tears, ectrodactyly, ectodermal dysplasia, and strange hair, skin and teeth [syndrome] |
| DMFT | Decayed, Missing and Filled Teeth |
|---|---|
| EPDS | Edinburgh Post Natal Depression Scale |
| PNA | post-natal age |
| P21 | post-natal day 21 |
| AHC | Adrenal hypoplasia congenita |
| pachyonychia congenita | A syndrome of ectodermal dysplasia of abnormal thickness and elevation of nail plates with palmar and plantar hyperkeratosis; the tongue is whitish and glazed owing to papillary atrophy; autosomal dominant inheritance. Synonym: Jadassohn-Lewandowski syndrome. (05 Mar 2000) |
|---|---|
| natal teeth | Predeciduous teeth present at birth. They may be well formed and normal or may represent hornified epithelial structures without roots. They are found on the gingivae over the crest of the ridge and arise from accessory buds of the dental lamina ahead of the deciduous buds or from buds of the accessory dental lamina. (12 Dec 1998) |
| pachyonychia | Abnormal thickness of the fingernails or toenails. Origin: pachy-+ G. Onyx, nail (05 Mar 2000) |
| natal | 1. Relating to birth. Origin: L. Natalis, fr. Nascor, pp. Natus, to be born 2. Relating to the buttocks or nates. Origin: L. Nates, buttocks (05 Mar 2000) |
| natal cleft | The sulcus between the buttocks (nates). Synonym: crena ani, anal cleft, crena clunium, gluteal cleft. (05 Mar 2000) |
| natal plum | <botany> The drupaceous fruit of two South African shrubs of the genus Arduina (A. Bispinosa and A. Grandiflora). Source: Websters Dictionary (01 Mar 1998) |
| Natal's sore | Lesion of cutaneous leishmaniasis. (05 Mar 2000) |
| natal tooth | A predeciduous supernumerary tooth present at birth. (05 Mar 2000) |
| amaurosis congenita of Leber | An autosomal recessive cone-rod abiotrophy causing blindness or severely reduced vision at birth. (05 Mar 2000) |
| amyoplasia congenita | Limitation of range of joint motion and contractures present at birth, usually involving multiple joints; a syndrome probably of diverse aetiology that may result from changes in spinal cord, muscle, or connective tissue. Several forms exist, autosomal dominant, recessive, and X-linked. Synonym: amyoplasia congenita. (05 Mar 2000) |
| amyotonia congenita | Atonic pseudoparalysis of congenital origin (neither familial nor hereditary), observed especially in infants and characterised by absences of muscular tone only in muscles innervated by the spinal nerves. Synonym: congenital atonic pseudoparalysis, myatonia congenita, Oppenheim's disease, Oppenheim's syndrome. An indefinite term for a number of congenital neuromuscular disorders that cause generalised myotonia in young children, and that have a benign course (static or regressive). (05 Mar 2000) |
| aplasia cutis congenita | Congenital absence or deficiency of a localised area of skin, with the base of the defect covered by a thin translucent membrane; most often a single area near the vertex of the scalp, but may occur in other areas; underlying structures may also be affected; autosomal inheritance, either dominant or recessive. (05 Mar 2000) |
| arthrogryposis multiplex congenita | Limitation of range of joint motion and contractures present at birth, usually involving multiple joints; a syndrome probably of diverse aetiology that may result from changes in spinal cord, muscle, or connective tissue. Several forms exist, autosomal dominant, recessive, and X-linked. Synonym: amyoplasia congenita. (05 Mar 2000) |
| chondrodystrophia calcificans congenita | A developmental error of the epiphyses characterised by severe deformities, epiphyses ossified from several discrete centres and with a stippled appearance, and thickened shafts of the long bones; congenital cataract and mental retardation are often present. There is an autosomal dominant form and an autosomal recessive form. Synonym: chondrodysplasia punctata, chondrodystrophia calcificans congenita, hypoplastic foetal chondrodystrophy, stippled epiphysis. (05 Mar 2000) |
| chondrodystrophia congenita punctata | Congenital shortening of the humerus and femur, with stippled epiphyses, high-arched palate, cataracts, erythroderma in the newborn, and scaling followed by follicular atrophoderma; there is also an autosomal dominant inheritance pattern . Synonym: chondrodystrophia congenita punctata. (05 Mar 2000) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|