26:5B-3 - Hereditary disorder defined
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.
Ā
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.
Ā
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