|
gptkb:Tay–Sachs_disease
|
gptkb:hexosaminidase_A
|
|
gptkb:Hurler_syndrome
|
gptkb:alpha-L-iduronidase
|
|
gptkb:MCAD_deficiency
|
medium-chain acyl-CoA dehydrogenase
|
|
gptkb:Tarui_disease
|
gptkb:phosphofructokinase
|
|
gptkb:phenylketonuria
|
gptkb:phenylalanine_hydroxylase
|
|
gptkb:glycogen_storage_disease_XII
|
gptkb:aldolase_A
|
|
gptkb:primary_hyperoxaluria_type_1
|
gptkb:alanine-glyoxylate_aminotransferase
|
|
gptkb:infantile_Gaucher's_disease
|
gptkb:glucocerebrosidase
|
|
gptkb:Type_2_Gaucher_disease
|
gptkb:glucocerebrosidase
|
|
gptkb:GABA_transaminase_deficiency
|
GABA transaminase (4-aminobutyrate aminotransferase)
|
|
gptkb:glycogen_storage_disease_type_XII
|
gptkb:aldolase_A
|
|
gptkb:hereditary_fructose_intolerance
|
gptkb:aldolase_B
|
|
gptkb:Glycogen_Storage_Disease_Type_V
|
myophosphorylase
|
|
gptkb:variegate_porphyria
|
gptkb:protoporphyrinogen_oxidase
|
|
gptkb:Gaucher_disease
|
gptkb:glucocerebrosidase
|
|
gptkb:Adenosine_deaminase_deficiency
|
gptkb:adenosine_deaminase
|
|
gptkb:AMP_deaminase_deficiency
|
gptkb:AMP_deaminase
|
|
gptkb:Andersen's_disease
|
glycogen branching enzyme
|
|
gptkb:MPS_IX
|
gptkb:hyaluronidase
|
|
gptkb:GM1_gangliosidosis_(in_humans)
|
gptkb:beta-galactosidase
|