Showing entry for Hereditary retinal dystrophy
| General Disease Information | |
|---|---|
| BXGD Id | BXGD003752 |
| Disease Name | Hereditary retinal dystrophy |
| Disease CUI Id | C0154860 |
| MeSH Codes | C16 C11 |
| Disease Class Name | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases |
| Semantic Type | Disease or Syndrome |
| Human Phenotype Ontology Id | |
| Human Phenotype Ontology Term | |
| Disease Ontology Id | DOID:630 DOID:7 DOID:225 |
| Disease Ontology Class Name | genetic disease; disease of anatomical entity; syndrome |
| Disorder Network | disorder-protein-compound-food associations
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