Showing entry for Ruvalcaba Syndrome
| General Disease Information | |
|---|---|
| BXGD Id | BXGD005481 |
| Disease Name | Ruvalcaba Syndrome |
| Disease CUI Id | C0265248 |
| MeSH Codes | C23 C16 C17 C05 C19 |
| Disease Class Name | Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Endocrine System 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
|