26:5B-3.Ā  Hereditary disorder defined
As used in this actĀ  "hereditary disorder"Ā  means any human ailment, diseaseĀ  or deformity resulting from a specific genetic condition and for whichĀ  treatment is available, and includes Cooley's anemia, cystic fibrosis, sickleĀ  cell anemia, hemophilia, Huntington's Disease, and inborn errors of metabolismĀ  such as galactosemia and phenylketonuria.

L.1981, c. 502, s. 3.
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