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nutrition disease
Summary
- Synonym
-
- Nutritional disorder
- Definition
- An acquired metabolic disease that is characterized by an insufficient intake of food or of certain nutrients, by an inability of the body to absorb and use nutrients, or by overconsumption of certain foods.
- Super Class
- acquired metabolic disease
External Links
- Disease Ontology
- DOID:374
- Mondo Disease Ontology
- MeSH
- UMLS
- NCI Thesaurus
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 3958 | LGALS3 | galectin 3 | |
| 3988 | LIPA | lipase A, lysosomal acid type | |
| 3992 | FADS1 | fatty acid desaturase 1 | |
| 5091 | PC | pyruvate carboxylase | |
| 5106 | PCK2 | phosphoenolpyruvate carboxykinase 2, mitochondrial | |
| 5290 | PIK3CA | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | |
| 5291 | PIK3CB | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta | |
| 5293 | PIK3CD | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta | |
| 5294 | PIK3CG | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma | |
| 5338 | PLD2 | phospholipase D2 |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q00796 | Sorbitol dehydrogenase | |
| Q10589 | Bone marrow stromal antigen 2 | |
| Q16822 | Phosphoenolpyruvate carboxykinase [GTP], mitochondrial | |
| Q6ZVN8 | Hemojuvelin | |
| Q8WWQ2 | Inactive heparanase-2 | |
| Q9C0K1 | Metal cation symporter ZIP8 | |
| Q9UEF7 | Klotho | |
| Q9UQE7 | Structural maintenance of chromosomes protein 3 |
