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| Term | vitamin metabolic disorder | ID (Ontology) | DOID:0050718 (Human Disease) |
| Definition | An inherited metabolic disorder resulting from a deficiency in vitamin or vitamin cofactor transport or metabolism. | ||
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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disease of metabolism__ genetic disease________| inherited metabolic disorder |__vitamin metabolic disorder 32 rec. |__autoinflammatory syndrome with cytopenia, hyperzincemia, and hypercalprotectinemia |__cerebral folate receptor alpha deficiency |__familial isolated deficiency of vitamin E 9 rec. |__glutamate formiminotransferase deficiency |__hereditary folate malabsorption 6 rec. |__pyridoxamine 5'-phosphate oxidase deficiency 10 rec. |__vitamin B12 deficiency 1 rec. |__congenital intrinsic factor deficiency 1 rec. |__transcobalamin II deficiency 1 rec. |
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| Is a | inherited metabolic disorder | ||
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