Alternative names (3)
deficiency causes • deficiencyLeadsTo • deficiencyOfRandom triples
Subject | Object |
---|---|
gptkb:fumarate_hydratase | neurological impairment |
gptkb:C1INH | gptkb:hereditary_hemorrhagic_telangiectasia |
gptkb:beta-hexosaminidase_A | gptkb:Tay-Sachs_disease |
gptkb:B6 | gptkb:anemia |
gptkb:HGH | dwarfism |
gptkb:pyruvate_carboxylase_enzyme | neurological dysfunction |
gptkb:B_6 | gptkb:depression |
gptkb:linoleic_acid_(LA) | scaly skin |
gptkb:glucosylceramidase_beta | gptkb:Gaucher_disease |
gptkb:pentose-phosphate_shunt | glucose-6-phosphate dehydrogenase deficiency |
gptkb:B6 | dermatitis |
gptkb:glutaryl-CoA_dehydrogenase | gptkb:glutaric_aciduria_type_I |
gptkb:Alpha-1_antitrypsin | gptkb:liver_disease |
gptkb:3β-hydroxysteroid_dehydrogenase | congenital adrenal hyperplasia |
gptkb:argininosuccinate_synthetase | gptkb:citrullinemia_type_I |
gptkb:B_6 | gptkb:anemia |
gptkb:MPS_I | gptkb:alpha-L-iduronidase |
gptkb:Sly_syndrome | beta-glucuronidase |
gptkb:pantothenic_acid_(vitamin_B5) | fatigue |
gptkb:carnitine_shuttle | impaired fatty acid oxidation |