Showing entry for Robinow Syndrome
| General Disease Information | |
|---|---|
| BXGD Id | BXGD005462 |
| Disease Name | Robinow Syndrome |
| Disease CUI Id | C0265205 |
| MeSH Codes | C16 C13 C05 C12 C19 |
| Disease Class Name | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Musculoskeletal Diseases; Male Urogenital Diseases; Endocrine System Diseases |
| Semantic Type | Disease or Syndrome |
| Human Phenotype Ontology Id | |
| Human Phenotype Ontology Term | |
| Disease Ontology Id | DOID:630 DOID:7 DOID:225 DOID:150 |
| Disease Ontology Class Name | genetic disease; disease of anatomical entity; syndrome; disease of mental health |
| Disorder Network | disorder-protein-compound-food associations
|