| ACD | 1) Absolute Cardiac Dullness; 절대심둔탁음 2) Anemia of Chronic Disease &nbs... |
|---|---|
| AD | 1) Alveolar Duct 2) Autosomal Dominant 3) Auris Dextra; Ri... |
| AR | 1) Aortic Regurgitation = AI Echo소견 &... |
| ABPA | actin-binding protein, autosomal form; allergic bronchopulmonary aspergillosis |
| ACHOO | autosomal dominant compelling helio-ophthalmic outburst [syndrome] |
| AD | Autosomal Dominant |
|---|---|
| ADCA | Autosomal Dominant Cerebellar Ataxia |
| ADPKD | Autosomal Dominant Polycystic Kidney Disease |
| AR | Autosomal Recessive |
| ADNFLE | Autosomal dominant nocturnal frontal lobe epilepsy |
| autosomal | Pertaining to an autosome. (05 Mar 2000) |
|---|---|
| autosomal dominant | <genetics> Requires only one affected parent have the trait to pass it to offspring. (02 Jan 1998) |
| 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 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) |
| 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) |
| autosomal |
of or relating to an autosome; "autosomal gene"
출처: wordnet.princeton.edu/perl/webwn
|
|---|---|
| autosomal |
affects both males and females equally.
출처: www.geocities.com/coloboma_group/words.html
|
| autosomal |
Everyone gets 1 chromozome from their mother and one from their father. The mother's chromozome is always an "X", and the father gives either an "X" (which causes a female child) or a "Y" (which causes a male child). If a disorder is autosomal it is found on both the x and y chromozomes.
출처: www.bdid.com/termsa.htm
|
| autosomal |
chromosomes other than sex chromosomes X, Y. (More? DNA Notes)
출처: embryology.med.unsw.edu.au/Notes/Index/A.htm
|
| autosomal |
Pertaining to a chromosome not involved in sex determination.
출처: plan2005.cancer.gov/glossary.html
|
| autosomal | of or relating to an autosome |
|---|---|
| autosomal | a disease caused by a dominant mutant gene on an autosome |
| autosomal | a disease caused by a dominant mutant gene on an autosome |
| autosomal | a disease caused by the presence of two recessive mutant genes on an autosome |
| autosomal | a disease caused by the presence of two recessive mutant genes on an autosome |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|