Preferred Name

Encephalopathy

ID

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C26920

ALT_DEFINITION

A functional and/or structural disorder of the brain that is acquired or congenital and characterised by mental and neurological symptoms.

Diffuse disease of the brain that alters function and/or structure of the brain and is characterized by an altered mental state.

A disorder characterized by a pathologic process involving the brain.

A disorder of the brain that can be caused by disease, injury, drugs, or chemicals.

code

C26920

Concept_In_Subset

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C191671

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C193006

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C177537

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C157711

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C193197

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C97150

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C189762

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C118464

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C191200

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C62596

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C191402

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C90259

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C191385

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C54450

Contributing_Source

MedDRA

ACC/AHA

NICHD

mCode

GDC

FDA

CTCAE

DEFINITION

A functional and/or structural disorder of the brain caused by diseases (e.g. liver disease, kidney disease), medications, chemicals, and injuries.

FDA_Table

Patient Code (Appendix B)

FULL_SYN

encephalopathy

Encephalopathy

Encephalopathy, unspecified

Is_Value_For_GDC_Property

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C177623

label

Encephalopathy

Legacy Concept Name

Encephalopathy

Maps_To

Encephalopathy

Preferred_Name

Encephalopathy

prefixIRI

Thesaurus:C26920

prefLabel

Encephalopathy

Semantic_Type

Disease or Syndrome

UMLS_CUI

C4013377

xRef

IMDRF:E0115

subClassOf

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C97154

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Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/OMIM/MTHU003333 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 LOOM
http://purl.obolibrary.org/obo/HP_0001298 Experimental Factor Ontology / 实验性因素本体 LOOM
http://purl.obolibrary.org/obo/HP_0001298 Human Phenotype Ontology / 人类表型本体 LOOM
http://purl.obolibrary.org/obo/HP_0001298 GenEpiO / 基因组流行病学本体 LOOM