Gaucher disease (GD) is a rare genetic disorder (1 in 75,000 births World-wide), an inborn error of metabolism due to a deficiency of the lysosomal enzyme acid β-glucosidase (glucocerebrosidase). Gaucher's Disease is a Prescribed Minimum Benefit condition under Diagnostic Treatment Pair (DTP) code 901K.
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Gaucher disease and pmbs.pdf | |