Showing entry for Central heterochromia
| General Disease Information | |
|---|---|
| BXGD Id | BXGD020676 |
| Disease Name | Central heterochromia |
| Disease CUI Id | C4021567 |
| MeSH Codes | C23 C11 C17 |
| Disease Class Name | Pathological Conditions, Signs and Symptoms; Eye Diseases; Skin and Connective Tissue Diseases |
| Semantic Type | Sign or Symptom |
| Human Phenotype Ontology Id | HP:0000478 |
| Human Phenotype Ontology Term | Abnormality of the eye |
| Disease Ontology Id | |
| Disease Ontology Class Name | |
| Disorder Network | disorder-protein-compound-food associations
|