Showing entry for Miller-McKusick-Malvaux-Syndrome (3M Syndrome)
| General Disease Information | |
|---|---|
| BXGD Id | BXGD014979 |
| Disease Name | Miller-McKusick-Malvaux-Syndrome (3M Syndrome) |
| Disease CUI Id | C1848862 |
| MeSH Codes | C23 C16 C05 C10 C19 |
| Disease Class Name | Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases; Endocrine System Diseases |
| Semantic Type | Disease or Syndrome |
| Human Phenotype Ontology Id | |
| Human Phenotype Ontology Term | |
| Disease Ontology Id | DOID:630 |
| Disease Ontology Class Name | genetic disease |
| Disorder Network | disorder-protein-compound-food associations
|