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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 |
|---|---|---|---|
| 38 | ACAT1 | acetyl-CoA acetyltransferase 1 | |
| 47 | ACLY | ATP citrate lyase | |
| 217 | ALDH2 | aldehyde dehydrogenase 2 family member | |
| 229 | ALDOB | aldolase, fructose-bisphosphate B | |
| 276 | AMY1A | amylase alpha 1A | |
| 277 | AMY1B | amylase alpha 1B | |
| 278 | AMY1C | amylase alpha 1C | |
| 684 | BST2 | bone marrow stromal cell antigen 2 | |
| 811 | CALR | calreticulin | |
| 847 | CAT | catalase |
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 |
