Showing entry for Heterotaxy, Visceral, 3, Autosomal
| General Disease Information | |
|---|---|
| BXGD Id | BXGD015336 |
| Disease Name | Heterotaxy, Visceral, 3, Autosomal |
| Disease CUI Id | C1853444 |
| 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 | |
| Human Phenotype Ontology Term | |
| Disease Ontology Id | DOID:0080015 |
| Disease Ontology Class Name | physical disorder |
| Disorder Network | disorder-protein-compound-food associations
|