Definition(s)
- A gene on one of the non-sex chromosomes that is always expressed, even if only one copy is present.
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Definition from: Human Genome Project Information
at the U.S. Department of Energy
- Describes
a trait or disorder in which the phenotype is expressed in those who have
inherited only one copy of a particular gene mutation (heterozygotes); specifically
refers to a gene on one of the 22 pairs of autosomes (non-sex chromosomes)
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More information from GeneTests
Definition from: GeneTests
from the University of Washington and Children's Health System, Seattle
Related discussion in the Handbook
See also Understanding Medical Terminology.