Showing entry for Insulin Receptor, Defect in
| General Disease Information | |
|---|---|
| BXGD Id | BXGD006237 |
| Disease Name | Insulin Receptor, Defect in |
| Disease CUI Id | C0271689 |
| MeSH Codes | C16 C18 C05 C19 |
| Disease Class Name | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Endocrine System Diseases |
| Semantic Type | Disease or Syndrome |
| Human Phenotype Ontology Id | |
| Human Phenotype Ontology Term | |
| Disease Ontology Id | DOID:630 |
| Disease Ontology Class Name | genetic disease |
| Disorder Network | disorder-protein-compound-food associations
|