FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term acquired metabolic disease ID (Ontology) DOID:0060158 (Human Disease)
Definition A disease of metabolism that has_material_basis_in enzyme deficiency or accumulation of enzymes or toxins which interfere with normal function due to an endocrine organ disease, organ malfunction, inadequate intake, dietary deficiency, or malabsorption.
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Data Class Field Records
Alleles (FBal)  HUMAN_DISEASE_INTERACTIONS       4
Human Disease Models (FBhh)  DOID       4
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 Alleles Genes Human Disease Models
 acquired metabolic disease       4      5      4
 model of | acquired metabolic disease       4       --       --
Spanning Tree (Parents/Children)
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  disease
   |__disease of metabolism
       |__acquired metabolic disease  246 rec.
           |__auto-brewery syndrome
           |__bladder fermentation syndrome
           |__carotenemia 1 rec.
           |__hyperprolactinemia
           |__hyperuricemia 13 rec.
           |   |__HRPT-related hyperuricemia
           |__metabolic acidosis 1 rec.
           |   |__alcoholic ketoacidosis
           |   |__diabetic ketoacidosis 1 rec.
           |   |__lactic acidosis
           |__mineral metabolism disease 19 rec.
           |   |__calcium metabolism disease(+) 15 rec.
           |   |__hypokalemia
           |   |__iron metabolism disease(+) 4 rec.
           |   |__phosphorus metabolism disease(+)
           |__nutrition disease 202 rec.
               |__nutritional deficiency disease(+)
               |__overnutrition(+) 202 rec.
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