- autosomal recessive trait
- 常染色体隐性遗传特性
Medical Chinese dictionary (湘雅医学词典). 2013.
autosomal recessive trait
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Autosomal recessive — A genetic condition that appears only in individuals who have received two copies of an autosomal gene, one copy from each parent. The gene is on an autosome, a nonsex chromosome. The parents are carriers who have only one copy of the gene and do … Medical dictionary
Medullary cystic kidney disease, autosomal recessive type — A childhood genetic kidney disease in which there is progressive symmetrical destruction of the kidneys involving both the tubules and glomeruli, characteristically resulting in anemia, polyuria, polydipsia, isosthenuria (decreased ability to… … Medical dictionary
Autosomal — Pertaining to a chromosome that is not a sex chromosome; relating to any one of the chromosomes save the sex chromosomes. People normally have 22 pairs of autosomes (44 autosomes) in each cell together with two sex chromosomes (X and Y in the… … Medical dictionary
Recessive, autosomal — A genetic condition that appears only in individuals who have received two copies of an autosomal gene, one copy from each parent. The gene is on an autosome, a nonsex chromosome. The parents are carriers who have only one copy of the gene and do … Medical dictionary
Recessive — A trait that is evident only when one copy of the gene for it is inherited from each of the parents. * * * 1. Drawing away; receding. 2. In genetics, denoting a trait due to a particular allele or alleles at a single locus that does not manifest… … Medical dictionary
phenylketonuria — Autosomal recessively inherited inborn error of metabolism of phenylalanine characterized by deficiency of 1) phenylalanine hydroxylase [MIM*261600] caused by mutation in the phenylalanine hydroxylase gene ( … Medical dictionary
syndrome — The aggregate of symptoms and signs associated with any morbid process, and constituting together the picture of the disease. SEE ALSO: disease. [G. s., a running together, tumultuous concourse; (in med.) a concurrence of symptoms, fr. syn,… … Medical dictionary
Progressive retinal atrophy — (PRA) is a group of genetic diseases seen in certain breeds of dogs and, more rarely, cats. It is characterized by the bilateral degeneration of the retina, causing progressive vision loss culminating in blindness. The condition in nearly all… … Wikipedia
Ehlers-Danlos syndrome — A heritable disorder of connective tissue with easy bruising, joint hypermobility (loose joints), skin laxity, and weakness of tissues. There are a number of different types of Ehlers Danlos syndrome (EDS) which share the foregoing features but… … Medical dictionary
Lethal white syndrome — (LWS), also called overo lethal white syndrome (OLWS), lethal white overo (LWO), and overo lethal white foal syndrome (OLWFS), is an autosomal genetic disorder most prevalent in the American Paint Horse. Affected foals are born after the full 11… … Wikipedia
Anemia — The condition of having less than the normal number of red blood cells or less than the normal quantity of hemoglobin in the blood. The oxygen carrying capacity of the blood is, therefore, decreased. Persons with anemia may feel tired and fatigue … Medical dictionary
