Showing entry for Omenn Syndrome
| General Disease Information | |
|---|---|
| BXGD Id | BXGD017472 |
| Disease Name | Omenn Syndrome |
| Disease CUI Id | C2700553 |
| MeSH Codes | C16 C18 C20 |
| Disease Class Name | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Immune System Diseases |
| Semantic Type | Disease or Syndrome |
| Human Phenotype Ontology Id | |
| Human Phenotype Ontology Term | |
| Disease Ontology Id | DOID:7 |
| Disease Ontology Class Name | disease of anatomical entity |
| Disorder Network | disorder-protein-compound-food associations
|