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 |