Alternative names (3)
deficiency causes • deficiencyLeadsTo • deficiencyOfRandom triples
| Subject | Object |
|---|---|
| gptkb:frataxin | oxidative stress |
| gptkb:L-phenylalanine | impaired protein synthesis |
| gptkb:Vitamin_K_group | bleeding disorders |
| gptkb:alpha1-proteinase_inhibitor | emphysema |
| gptkb:Adenosine_Deaminase_Severe_Combined_Immunodeficiency | adenosine deaminase enzyme |
| gptkb:Vitamin_K1 | bleeding disorders |
| gptkb:Vitamin_K2 | gptkb:bone |
| gptkb:coenzyme_Q10 | muscle weakness |
| gptkb:McArdle_disease | muscle glycogen phosphorylase |
| gptkb:leptin | obesity |
| gptkb:tenascin-X | skin hyperextensibility |
| gptkb:Mucopolysaccharidosis_type_II | gptkb:iduronate-2-sulfatase |
| gptkb:muscle-type_aldolase | gptkb:glycogen_storage_disease_type_XII |
| gptkb:succinate_semialdehyde_dehydrogenase | succinic semialdehyde dehydrogenase deficiency |
| gptkb:CPS-1 | hyperammonemia |
| gptkb:B_1 | gptkb:Wernicke-Korsakoff_syndrome |
| gptkb:fibrinogen | dysfibrinogenemia |
| gptkb:Albumins | Edema |
| gptkb:B6 | gptkb:depression |
| gptkb:Alpha-L-iduronidase | gptkb:Mucopolysaccharidosis_type_I |