Alternative names (3)
deficiency causes • deficiencyLeadsTo • deficiencyOfRandom triples
| Subject | Object |
|---|---|
| gptkb:histidine_ammonia-lyase | histidinemia |
| gptkb:B_6 | gptkb:anemia |
| gptkb:coagulation_factor_XI | gptkb:hemophilia_C |
| gptkb:Vitamin_B12 | neurological problems |
| gptkb:MPS_VI | arylsulfatase B enzyme |
| gptkb:complement_protein_C3 | increased susceptibility to bacterial infections |
| gptkb:carnitine_shuttle | impaired fatty acid oxidation |
| gptkb:Vitamin_B7 | skin rash |
| gptkb:GM2_gangliosidosis,_type_I | gptkb:hexosaminidase_A |
| gptkb:cystathionase | cystathioninuria |
| gptkb:omega_fatty_acids | impaired growth |
| gptkb:all-trans-retinol | impaired immunity |
| gptkb:N-acetyl-beta-hexosaminidase_A | gptkb:Tay-Sachs_disease |
| gptkb:menaquinone_(K2) | arterial calcification |
| gptkb:all-trans-retinol | xerophthalmia |
| gptkb:Lesch–Nyhan_syndrome | gptkb:hypoxanthine-guanine_phosphoribosyltransferase |
| gptkb:Manganese_superoxide_dismutase | neurodegeneration |
| gptkb:Leucine | headaches |
| gptkb:adenosine_deaminase | gptkb:severe_combined_immunodeficiency_(SCID) |
| gptkb:mucopolysaccharidosis_type_I_(MPS_I) | gptkb:alpha-L-iduronidase |