Showing entry for Transthyretin related familial amyloid cardiomyopathy
| General Disease Information | |
|---|---|
| BXGD Id | BXGD022362 |
| Disease Name | Transthyretin related familial amyloid cardiomyopathy |
| Disease CUI Id | C4275067 |
| MeSH Codes | C16 C18 |
| Disease Class Name | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic 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
|