Showing entry for Marcus Gunn phenomenon
| General Disease Information | |
|---|---|
| BXGD Id | BXGD005685 |
| Disease Name | Marcus Gunn phenomenon |
| Disease CUI Id | C0266521 |
| MeSH Codes | C23 C16 C11 C05 C10 C07 C14 |
| Disease Class Name | Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Musculoskeletal Diseases; Nervous System Diseases; Stomatognathic Diseases; Cardiovascular Diseases |
| Semantic Type | Disease or Syndrome |
| Human Phenotype Ontology Id | HP:0000478 |
| Human Phenotype Ontology Term | Abnormality of the eye |
| Disease Ontology Id | DOID:7 |
| Disease Ontology Class Name | disease of anatomical entity |
| Disorder Network | disorder-protein-compound-food associations
|