Showing entry for Arrhinia
| General Disease Information | |
|---|---|
| BXGD Id | BXGD005572 |
| Disease Name | Arrhinia |
| Disease CUI Id | C0265740 |
| MeSH Codes | C16 |
| Disease Class Name | Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| Semantic Type | Congenital Abnormality |
| Human Phenotype Ontology Id | HP:0000152 |
| Human Phenotype Ontology Term | Abnormality of head or neck |
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| Disorder Network | disorder-protein-compound-food associations |
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