Showing entry for Singleton Merten syndrome
| General Disease Information | |
|---|---|
| BXGD Id | BXGD008757 |
| Disease Name | Singleton Merten syndrome |
| Disease CUI Id | C0432254 |
| MeSH Codes | C16 C18 C05 C10 C07 C14 |
| Disease Class Name | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases; Stomatognathic 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
|