Showing entry for Congenital glucose-galactose malabsorption
| General Disease Information | |
|---|---|
| BXGD Id | BXGD005848 |
| Disease Name | Congenital glucose-galactose malabsorption |
| Disease CUI Id | C0268186 |
| MeSH Codes | C16 C06 C18 |
| Disease Class Name | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases |
| Semantic Type | Disease or Syndrome; Congenital Abnormality |
| Human Phenotype Ontology Id | |
| Human Phenotype Ontology Term | |
| Disease Ontology Id | |
| Disease Ontology Class Name | |
| Disorder Network | disorder-protein-compound-food associations |
| The disease-related target proteins | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Proteins |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| The disease-related compounds | ||||||
| Compounds |
|
|||||
| The disease-related foods | ||||||
| Foods |
|
|||||
