Alternative names (3)
deficiency causes • deficiencyLeadsTo • deficiencyOfRandom triples
| Subject | Object |
|---|---|
| gptkb:vitamin_K2_(menaquinone) | gptkb:bone |
| gptkb:antithrombin_III | increased risk of thrombosis |
| gptkb:Leucine | headaches |
| gptkb:beta-hexosaminidase_A | gptkb:Tay-Sachs_disease |
| gptkb:Vitamin_B9 | neural tube defects |
| gptkb:Factor_I | complement factor I deficiency |
| gptkb:Manganese_superoxide_dismutase | gptkb:cardiomyopathy |
| gptkb:pyruvate_carboxylase_enzyme | neurological dysfunction |
| gptkb:muscle_phosphoglycerate_mutase | glycogen storage disease type X |
| gptkb:pyridoxine_(vitamin_B6) | gptkb:dermatitis |
| gptkb:adenosine_deaminase | gptkb:severe_combined_immunodeficiency_(SCID) |
| gptkb:linoleic_acid_(LA) | scaly skin |
| gptkb:Histidine_ammonia-lyase | histidinemia |
| gptkb:Riboflavin-lactoflavin | gptkb:ariboflavinosis |
| gptkb:alpha1-proteinase_inhibitor | emphysema |
| gptkb:carnitine | gptkb:cardiomyopathy |
| gptkb:pyridoxine_(vitamin_B6) | confusion |
| gptkb:carnitine_shuttle | impaired fatty acid oxidation |
| gptkb:coagulation_factor_X | gptkb:bleeding_disorder |
| gptkb:MPS_VI | arylsulfatase B enzyme |