Tay-Sachs disease | recessive disorder that results from the absence of an enzyme required to break down lipids |
Huntington's disease | Lethal genetic disorder caused by a dominant allele |
cystic fibrosis | most common genetic disorder among white Americans |
phenylketonuria | recessive disorder that results from the absence of an enzyme that converts one amino acid into another one |
simple dominant traits | window's peak and hitch hiker's thumb |
pedigree | graphic representation of genetic inheritance |
carrier | heterozygous individual |
autosomes | 22 pairs of homologous chromosomes in males and females |
sex chromosomes | 23rd pair of chromosomes that are different in males and females |
codominant alleles | both phenotypes produced in heterozygote |
incomplete dominance | phenotype of heterozygous individual is intermediate between those of homozygous |
XX | female |
XY | male |
karyotype | chart of chromosome pairs prepared from photo of metaphase |
fetus | developing baby inside the mother |
multiple alleles | traits controlled by more than 2 alleles |
sex-linked traits | traits controlled by genes located on sex chromosomes |
polygenic inheritance | the inheritance pattern of a trait that is controlled by two or more genes |