Showing entry for Deafness, Congenital Heart Defects, and Posterior Embryotoxon
| General Disease Information | |
|---|---|
| BXGD Id | BXGD016367 |
| Disease Name | Deafness, Congenital Heart Defects, and Posterior Embryotoxon |
| Disease CUI Id | C1866053 |
| MeSH Codes | C23 C16 C10 C09 C14 |
| Disease Class Name | Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Otorhinolaryngologic Diseases; Cardiovascular Diseases |
| Semantic Type | Disease or Syndrome |
| Human Phenotype Ontology Id | |
| Human Phenotype Ontology Term | |
| Disease Ontology Id | |
| Disease Ontology Class Name | |
| Disorder Network | disorder-protein-compound-food associations
|