Preferred Name

Syndrome

ID

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C28193

ALT_DEFINITION

A set of symptoms or conditions that occur together and suggest the presence of a certain disease or an increased chance of developing the disease.

code

C28193

Concept_In_Subset

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

Contributing_Source

NICHD

DEFINITION

A group of signs, symptoms, and clinicopathological characteristics that may or may not have a genetic basis and collectively define an abnormal condition.

FULL_SYN

syndrome

Syndrome

label

Syndrome

Legacy Concept Name

Syndrome

Preferred_Name

Syndrome

prefixIRI

Thesaurus:C28193

prefLabel

Syndrome

Semantic_Type

Disease or Syndrome

UMLS_CUI

C0039082

subClassOf

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C2991

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http://purl.obolibrary.org/obo/DOID_225 BioAssay Ontology / 生物活性分析本体 LOOM
http://purl.obolibrary.org/obo/DOID_225 Ontology of Drug Adverse Events / 药物不良反应本体 LOOM
http://purl.obolibrary.org/obo/DOID_225 Human Disease Ontology / 人类疾病本体 LOOM
http://purl.bioontology.org/ontology/MESH/D013577 Medical Subject Headings / 医学主题词表 LOOM
http://semanticscience.org/resource/SIO_001017 Semanticscience Integrated Ontology / 语义科学集成本体 LOOM
http://purl.obolibrary.org/obo/NCIT_C28193 GenEpiO / 基因组流行病学本体 LOOM
http://purl.obolibrary.org/obo/OGMS_0000086 Ontology for General Medical Science / 通用医学科学本体 LOOM