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 |