Showing entry for Uhl anomaly
| General Disease Information | |
|---|---|
| BXGD Id | BXGD005582 |
| Disease Name | Uhl anomaly |
| Disease CUI Id | C0265857 |
| MeSH Codes | C16 C14 |
| Disease Class Name | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases |
| Semantic Type | Congenital Abnormality |
| Human Phenotype Ontology Id | HP:0001626 |
| Human Phenotype Ontology Term | Abnormality of the cardiovascular system |
| Disease Ontology Id | DOID:630 DOID:7 |
| Disease Ontology Class Name | genetic disease; disease of anatomical entity |
| Disorder Network | disorder-protein-compound-food associations
|