Showing entry for Usher Syndrome, Type II
| General Disease Information | |
|---|---|
| BXGD Id | BXGD013420 |
| Disease Name | Usher Syndrome, Type II |
| Disease CUI Id | C1568249 |
| MeSH Codes | C23 C16 C11 C10 C09 |
| Disease Class Name | Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nervous System Diseases; Otorhinolaryngologic Diseases |
| Semantic Type | Disease or Syndrome |
| Human Phenotype Ontology Id | |
| Human Phenotype Ontology Term | |
| Disease Ontology Id | DOID:630 DOID:225 |
| Disease Ontology Class Name | genetic disease; syndrome |
| Disorder Network | disorder-protein-compound-food associations
|