Showing entry for Asplenia Syndrome
| General Disease Information | |
|---|---|
| BXGD Id | BXGD004011 |
| Disease Name | Asplenia Syndrome |
| Disease CUI Id | C0175707 |
| MeSH Codes | C16 C15 C14 |
| Disease Class Name | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases; Cardiovascular Diseases |
| Semantic Type | Disease or Syndrome |
| Human Phenotype Ontology Id | HP:0001507 |
| Human Phenotype Ontology Term | Growth abnormality |
| Disease Ontology Id | DOID:630 DOID:0080015 |
| Disease Ontology Class Name | genetic disease; physical disorder |
| Disorder Network | disorder-protein-compound-food associations
|