Showing entry for Apraxia, oculomotor, Cogan type
| General Disease Information | |
|---|---|
| BXGD Id | BXGD009299 |
| Disease Name | Apraxia, oculomotor, Cogan type |
| Disease CUI Id | C0543874 |
| MeSH Codes | C23 C11 C10 F01 C14 |
| Disease Class Name | Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases; Behavior and Behavior Mechanisms; Cardiovascular Diseases |
| Semantic Type | Congenital Abnormality |
| Human Phenotype Ontology Id | |
| Human Phenotype Ontology Term | |
| Disease Ontology Id | DOID:7 |
| Disease Ontology Class Name | disease of anatomical entity |
| Disorder Network | disorder-protein-compound-food associations
|