Showing entry for Synophrys
| General Disease Information | |
|---|---|
| BXGD Id | BXGD008690 |
| Disease Name | Synophrys |
| Disease CUI Id | C0431447 |
| MeSH Codes | C16 C17 |
| Disease Class Name | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases |
| Semantic Type | Congenital Abnormality |
| Human Phenotype Ontology Id | HP:0001574 HP:0000152 |
| Human Phenotype Ontology Term | Abnormality of the integument; Abnormality of head or neck |
| Disease Ontology Id | |
| Disease Ontology Class Name | |
| Disorder Network | disorder-protein-compound-food associations
|