Showing entry for Pierre Robin syndrome with fetal chondrodysplasia
| General Disease Information | |
|---|---|
| BXGD Id | BXGD014930 |
| Disease Name | Pierre Robin syndrome with fetal chondrodysplasia |
| Disease CUI Id | C1848488 |
| MeSH Codes | C16 C05 C07 |
| Disease Class Name | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Stomatognathic 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
|