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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 |
|---|---|---|---|
| 2538 | G6PC1 | glucose-6-phosphatase catalytic subunit 1 | |
| 2542 | SLC37A4 | solute carrier family 37 member 4 | |
| 2572 | GAD2 | glutamate decarboxylase 2 | |
| 2592 | GALT | galactose-1-phosphate uridylyltransferase | |
| 2720 | GLB1 | galactosidase beta 1 | |
| 2878 | GPX3 | glutathione peroxidase 3 | |
| 3283 | HSD3B1 | hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 1 | |
| 3383 | ICAM1 | intercellular adhesion molecule 1 | |
| 3938 | LCT | lactase | |
| 3939 | LDHA | lactate dehydrogenase A |
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 |
