Sphingolipidosis,Pathologic Nystagmus,Kluver-Bucy Syndrome,Mucopolysaccharidosis Iii,Mucopolysaccharidosis-Plus Syndrome,Mucopolysaccharidosis Iv,Fundus Dystrophy,Tay-Sachs Disease,Diarrhea,Lysosomal Storage Disease,Mucopolysaccharidoses,Pityriasis Rubra Pilaris,Gm1 Gangliosidosis,Neuronal Ceroid Lipofuscinosis,Ceroid Lipofuscinosis, Neuronal, 10,Disease Of Mental Health,Ceroid Lipofuscinosis, Neuronal, 7,Krabbe Disease,Hurler-Scheie Syndrome,Scheie Syndrome,Mannosidosis, Alpha B, Lysosomal,Metachromatic Leukodystrophy,Ceroid Lipofuscinosis, Neuronal, 3,Mucopolysaccharidosis, Type Ii,Mucopolysaccharidosis, Type Iiia,Mucopolysaccharidosis, Type Iiib,Mucopolysaccharidosis, Type Iiic,Mucopolysaccharidosis, Type Iiid,Mucopolysaccharidosis, Type Iva,Mucopolysaccharidosis, Type Ivb,Mucopolysaccharidosis, Type Vii,Ceroid Lipofuscinosis, Neuronal, 1

Mucopolysaccharidosis Iii,Mucopolysaccharidosis-Plus Syndrome,Mucopolysaccharidosis Iv,Sudden Infant Death Syndrome,Tay-Sachs Disease,Lysosomal Storage Disease,Refractory Cytopenia With Multilineage Dysplasia,Gm1-Gangliosidosis, Type Ii,Krabbe Disease,Hurler Syndrome,Epidermolysis Bullosa Simplex With Nail Dystrophy,Scheie Syndrome,Metachromatic Leukodystrophy,Mucopolysaccharidosis, Type Ii,Mucopolysaccharidosis, Type Iiia,Mucopolysaccharidosis, Type Iiib,Mucopolysaccharidosis, Type Iiic,Mucopolysaccharidosis, Type Iiid,Mucopolysaccharidosis, Type Iva,Mucopolysaccharidosis, Type Ivb,Mucopolysaccharidosis, Type Vi,Mucopolysaccharidosis, Type Vii

Ichthyosis,Endometrial Cancer,Chondrodysplasia Punctata Syndrome,Myopathy, Myosin Storage, Autosomal Dominant,Amelogenesis Imperfecta,Smith-Lemli-Opitz Syndrome,Cryptorchidism, Unilateral Or Bilateral,Multiple Sulfatase Deficiency,Endometriosis,Corneal Dystrophy, Thiel-Behnke Type,Epidermolytic Hyperkeratosis,Pre-Descemet Corneal Dystrophy,Breast Cancer,Kallmann Syndrome,Skin Disease,Periventricular Nodular Heterotopia,Ocular Albinism,Attention Deficit-Hyperactivity Disorder,Metachromatic Leukodystrophy,Ichthyosis Vulgaris,Ichthyosis, X-Linked,Autosomal Recessive Congenital Ichthyosis

Bone Development Disease,Zellweger Syndrome,Mucolipidosis,Morquio Syndrome,Gangliosidosis,Osteochondrosis,Mucopolysaccharidosis Iii,Mucopolysaccharidosis-Plus Syndrome,Mucopolysaccharidosis Iv,Multiple Sulfatase Deficiency,Dyggve-Melchior-Clausen Disease,Lysosomal Storage Disease,Tracheal Disease,Isolated Growth Hormone Deficiency, Type Ii,Gm1 Gangliosidosis,Glycoproteinosis,Fucosidosis,Odontochondrodysplasia,Spondyloepiphyseal Dysplasia With Congenital Joint Dislocations,Hurler Syndrome,Hurler-Scheie Syndrome,Scheie Syndrome,Adenine Phosphoribosyltransferase Deficiency,Legg-Calve-Perthes Disease,Mucolipidosis Ii Alpha/Beta,Mucopolysaccharidosis, Type Ii,Mucopolysaccharidosis, Type Iiia,Mucopolysaccharidosis, Type Iiib,Mucopolysaccharidosis, Type Iiic,Mucopolysaccharidosis, Type Iiid,Mucopolysaccharidosis, Type Iva,Mucopolysaccharidosis, Type Ivb,Mucopolysaccharidosis, Type Vi,Mucopolysaccharidosis, Type Vii,Tracheomalacia,Galactosialidosis

Ichthyosis,Mucolipidosis,Gaucher'S Disease,Sphingolipidosis,Dysostosis,Cerebral Palsy,Lipid Storage Disease,Sandhoff Disease,Kleptomania,Mucopolysaccharidosis Iii,Mucopolysaccharidosis-Plus Syndrome,Mucopolysaccharidosis Iv,Canavan Disease,Multiple Sulfatase Deficiency,Hereditary Dystonia,Dementia,Autosomal Recessive Sideroblastic Anemia,Gingival Hypertrophy,Tay-Sachs Disease,Leukodystrophy,Polyneuropathy,Spinocerebellar Ataxia, Autosomal Recessive 14,Metachromatic Leukodystrophy, Adult Form,Metachromatic Leukodystrophy, Late Infantile Form,Metachromatic Leukodystrophy, Juvenile Form,Lysosomal Storage Disease,Demyelinating Disease,Gm2 Gangliosidosis,Gm1 Gangliosidosis,Sneddon Syndrome,Combined Saposin Deficiency,Autosomal Recessive Disease,Krabbe Disease,Fabry Disease,Scheie Syndrome,Metachromatic Leukodystrophy,Mucolipidosis Iii Alpha/Beta,Ceroid Lipofuscinosis, Neuronal, 3,Mucopolysaccharidosis, Type Ii,Mucopolysaccharidosis, Type Iiia,Mucopolysaccharidosis, Type Iva,Mucopolysaccharidosis, Type Vi,Mucopolysaccharidosis, Type Vii,Niemann-Pick Disease, Type C1