Definition(s)
- Describes
a trait or disorder requiring the presence of two copies of a gene mutation
at a particular locus in order to express observable phenotype; specifically
refers to genes 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.