Showing entry for Fabry Disease
| General Disease Information | |
|---|---|
| BXGD Id | BXGD000165 |
| Disease Name | Fabry Disease |
| Disease CUI Id | C0002986 |
| MeSH Codes | C16 C18 C10 C14 |
| Disease Class Name | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases; Cardiovascular Diseases |
| Semantic Type | Disease or Syndrome |
| Human Phenotype Ontology Id | HP:0001574 HP:0001626 |
| Human Phenotype Ontology Term | Abnormality of the integument; Abnormality of the cardiovascular system |
| Disease Ontology Id | DOID:0014667 DOID:630 |
| Disease Ontology Class Name | disease of metabolism; genetic disease |
| Disorder Network | disorder-protein-compound-food associations
|