| Preferred Name |
Liver Dysfunction |
| ID |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C50634 |
| code |
C50634 |
| Concept_In_Subset | |
| Contributing_Source |
FDA |
| DEFINITION |
A finding that indicates abnormal liver function. |
| FDA_Table |
Patient Code (Appendix B) |
| FULL_SYN |
Dysfunction, Liver |
| Has_CDRH_Parent | |
| label |
Liver Dysfunction |
| Legacy_Concept_Name |
Liver_Dysfunction |
| Preferred_Name |
Liver Dysfunction |
| prefixIRI |
C50634 |
| prefLabel |
Liver Dysfunction |
| Semantic_Type |
Finding |
| UMLS_CUI |
C0086565 |
| subClassOf |
| Delete | Mapping To | Ontology | Source |
|---|---|---|---|
| http://purl.bioontology.org/ontology/OMIM/MTHU013529 | Online Mendelian Inheritance in Man | LOOM |