| ACD | 1) Absolute Cardiac Dullness; 절대심둔탁음 2) Anemia of Chronic Disease &nbs... |
|---|---|
| AD | 1) Alveolar Duct 2) Autosomal Dominant 3) Auris Dextra; Ri... |
| ACHOO | autosomal dominant compelling helio-ophthalmic outburst [syndrome] |
| AD | accident dispensary; acetate dialysis; active disease; acute dermatomyositis; addict, addiction; ade... |
| ADPKD | autosomal dominant polycystic kidney disease |
| AD | Autosomal Dominant |
|---|---|
| ADCA | Autosomal Dominant Cerebellar Ataxia |
| ADPKD | Autosomal Dominant Polycystic Kidney Disease |
| ADNFLE | Autosomal dominant nocturnal frontal lobe epilepsy |
| ADRP | Autosomal dominant retinitis pigmentosa |
| autosomal dominant | <genetics> Requires only one affected parent have the trait to pass it to offspring. (02 Jan 1998) |
|---|---|
| kidney, polycystic, autosomal dominant | A genetic disorder with autosomal dominant inheritance characterised by multiple cysts in both kidneys and progressive deterioration of renal function. It is usually caused by a mutant gene at the pkd1 locus on the short arm of chromosome 16, though mutations elsewhere in the genome can also cause the disease. The age of onset of symptoms varies widely. (12 Dec 1998) |
| autosomal | Pertaining to an autosome. (05 Mar 2000) |
| autosomal gene | A gene located on any chromosome other than the sex chromosomes (X or Y). (05 Mar 2000) |
| autosomal recessive | <genetics> Mutation carried on an autosome that is deleterious only in homozygotes. (02 Jan 1998) |
| recessive, autosomal | A gene on a nonsex chromosome (an autosome) that expresses itself only when there is no different gene present at that locus (spot on the chromosome). For example, cystic fibrosis (cf) is an autosomal recessive disorder. A cf child has the cf gene on both chromosome 7's (and so is said to be homozygous for cf). (12 Dec 1998) |
| kidney, polycystic, autosomal recessive | Rare genetic disorder with autosomal recessive inheritance characterised by multiple cysts in both kidneys and associated hepatic lesions. Serious manifestations are usually present at birth and there is high perinatal mortality. (12 Dec 1998) |
| macular drusen | Excrescences of Bruch's membrane that produce a window in the retinal pigment epithelium and are a feature of age-related macular retinal degeneration. Synonym: macular drusen. (05 Mar 2000) |
| giant drusen | An obsolete term for a glial hamartoma of the optic nerve head or the peripapillary retina, seen in tuberous sclerosis. (05 Mar 2000) |
| retinal drusen | <ophthalmology> Colloid or hyaline bodies lying beneath the retinal pigment epithelium. They may occur either secondary to changes in the choroid that affect the pigment epithelium or as an autosomal dominant disorder of the retinal pigment epithelium. (12 Dec 1998) |
| drusen | Small bright structures seen in the retina and in the optic disc. Origin: Ger. Pl. Of druse, stony nodule, geode (05 Mar 2000) |
| drusen of the macula | Excrescences of Bruch's membrane that produce a window in the retinal pigment epithelium and are a feature of age-related macular retinal degeneration. Synonym: macular drusen. (05 Mar 2000) |
| drusen of the optic nerve head | Basophilic, laminated, calcareous acellular masses that resemble crystals within the nerve head, anterior to the lamina cribrosa, that may simulate papilledema and/or cause visual field defects. Synonym: intrapapillary drusen. (05 Mar 2000) |
| intrapapillary drusen | Basophilic, laminated, calcareous acellular masses that resemble crystals within the nerve head, anterior to the lamina cribrosa, that may simulate papilledema and/or cause visual field defects. Synonym: intrapapillary drusen. (05 Mar 2000) |
| optic disk drusen | Hyaline bodies occurring in the intra-ocular portion of the optic nerve. They are distinguished from retinal drusen, which lie beneath the retinal pigment epithelium. This disorder is differentiated also from papilledema by the absence of dilated retinal vessels. (12 Dec 1998) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|