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gptkb:Andersen's_disease
|
glycogen branching enzyme
|
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gptkb:Adenosine_deaminase_deficiency
|
gptkb:adenosine_deaminase
|
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gptkb:Triosephosphate_isomerase_deficiency
|
gptkb:triosephosphate_isomerase
|
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gptkb:glycogen_storage_disease_type_XII
|
gptkb:aldolase_A
|
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gptkb:hereditary_coproporphyria
|
gptkb:coproporphyrinogen_oxidase
|
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gptkb:MCADD
|
medium-chain acyl-CoA dehydrogenase
|
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gptkb:glycogen_storage_disease_XII
|
gptkb:aldolase_A
|
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gptkb:Type_2_Gaucher_disease
|
gptkb:glucocerebrosidase
|
|
gptkb:Glycogen_Storage_Disease_Type_V
|
myophosphorylase
|
|
gptkb:GABA_transaminase_deficiency
|
GABA transaminase (4-aminobutyrate aminotransferase)
|
|
gptkb:Tay–Sachs_disease
|
gptkb:hexosaminidase_A
|
|
gptkb:GABA-transaminase_deficiency
|
gptkb:GABA_transaminase
|
|
gptkb:Cori_disease
|
glycogen debranching enzyme
|
|
gptkb:Gaucher_disease
|
gptkb:glucocerebrosidase
|
|
gptkb:Tarui_disease
|
gptkb:phosphofructokinase
|
|
gptkb:primary_hyperoxaluria_type_1
|
gptkb:alanine-glyoxylate_aminotransferase
|
|
gptkb:acute_intermittent_porphyria
|
porphobilinogen deaminase
|
|
gptkb:glycogen_storage_disease_type_VII
|
gptkb:phosphofructokinase
|
|
gptkb:MCAD_deficiency
|
medium-chain acyl-CoA dehydrogenase
|
|
gptkb:GM1_gangliosidosis_(in_humans)
|
gptkb:beta-galactosidase
|