| Preferred Name |
Loss of Vision |
| ID |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C50638 |
| code |
C50638 |
| Concept_In_Subset | |
| Contributing_Source |
FDA |
| FDA_Table |
Patient Code (Appendix B) |
| FULL_SYN |
Vision, Loss Of |
| Has_CDRH_Parent | |
| label |
Loss of Vision |
| Legacy_Concept_Name |
Loss_Of_Vision |
| Preferred_Name |
Loss of Vision |
| prefixIRI |
C50638 |
| prefLabel |
Loss of Vision |
| Semantic_Type |
Finding |
| UMLS_CUI |
C3665346 |
| subClassOf |
| Delete | Mapping To | Ontology | Source |
|---|---|---|---|
| http://purl.bioontology.org/ontology/OMIM/MTHU001331 | Online Mendelian Inheritance in Man | LOOM | |
| http://purl.obolibrary.org/obo/SYMP_0000321 | Human Disease Ontology 123 | LOOM |