Provides comprehensive treatment for patients of all ages with Lysomal Storage Diseases, such as Gaucher Disease, Pompe Disease, Fabry Disease, and Mucopolysaccharide Storage Diseases. Provides all the components of care for patients and their families from initial consultation, testing and diagnosis to follow-up and treatment as well as genetic counseling, carrier screening and prenatal diagnosis.

Certain inherited diseases occur more frequently in a given ethnic or racial group than in the general population. The Jewish Genetic Disease Program provides education, genetic screening, genetic counseling and clinical services for individuals or families commonly affected by these diseases. Fanconi Anemia (Type C), Tay-Sachs Disease, Canavan Diseases, Niemann-Pick Disease, Bloom Syndrome,Mucolipodosis (Type lV), Gaucher Disease (Type l), Familial Dysautonomia and Cystic Fibrosis are among the many genetic diseases that have been tested.