Showing entry for Ablepharon
| General Disease Information | |
|---|---|
| BXGD Id | BXGD005697 |
| Disease Name | Ablepharon |
| Disease CUI Id | C0266574 |
| MeSH Codes | C16 C11 |
| Disease Class Name | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases |
| Semantic Type | Congenital Abnormality |
| Human Phenotype Ontology Id | HP:0000152 |
| Human Phenotype Ontology Term | Abnormality of head or neck |
| Disease Ontology Id | |
| Disease Ontology Class Name | |
| Disorder Network | disorder-protein-compound-food associations
|