- autosomal dominant trait
- 보통염색체우성소질
English-Korean animal medical dictionary. 2013.
autosomal dominant trait
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Autosomal dominant — A gene on one of the autosomes (non sex chromosomes) that, if present, will almost always produce a specific trait or disease. An autosomal dominant disorder can be inherited when only one parent passes on the gene. The chance of passing the gene … Medical dictionary
Dominant — A genetic trait is considered dominant if it is expressed in a person who has only one copy of that gene. (In genetic terms, a dominant trait is one that is phenotypically expressed in heterozygotes). A dominant trait is opposed to a recessive… … 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
Dominant white — This dominant white Thoroughbred stallion (W2/+) has one form of dominant white. His skin, hooves, and coat lack pigment cells, giving him a pink skinned white coat. Dominant white is a group of genetically related coat color conditions in the… … Wikipedia
Polykystose renale type dominant — Polykystose rénale type dominant Pour les articles homonymes, voir PKD. Polykystose rénale type dominant … Wikipédia en Français
Polykystose rénale type dominant — Pour les articles homonymes, voir PKD. Polykystose rénale type dominant Référence MIM 173900 173910 601313 … Wikipédia en Français
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
Human genetics — describes the study of inheritance as it occurs in human beings. Human genetics encompasses a variety of overlapping fields including: classical genetics, cytogenetics, molecular genetics, biochemical genetics, genomics, population genetics,… … 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
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
Syndrome, Ehlers-Danlos — 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
