Showing entry for Pierre Robin Syndrome
| General Disease Information | |
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| BXGD Id | BXGD002313 |
| Disease Name | Pierre Robin Syndrome |
| Disease CUI Id | C0031900 |
| MeSH Codes | C16 C05 C07 |
| Disease Class Name | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Stomatognathic Diseases |
| Semantic Type | Congenital Abnormality |
| Human Phenotype Ontology Id | HP:0000152 |
| Human Phenotype Ontology Term | Abnormality of head or neck |
| Disease Ontology Id | DOID:630 DOID:7 DOID:225 |
| Disease Ontology Class Name | genetic disease; disease of anatomical entity; syndrome |
| Disorder Network | disorder-protein-compound-food associations |
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