National Cancer Institute Thesaurus

Last uploaded: February 21, 2019
Preferred Name

Hyperthyroidism

ID

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C3123

ALT_DEFINITION

Too much thyroid hormone. Symptoms include weight loss, chest pain, cramps, diarrhea, and nervousness.

A disorder characterized by excessive levels of thyroid hormone in the body. Common causes include an overactive thyroid gland or thyroid hormone overdose.

Overproduction of thyroid hormone.

code

C3123

Concept_In_Subset

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

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

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C99147

Contributing_Source

NICHD

MedDRA

DEFINITION

Overactivity of the thyroid gland resulting in overproduction of thyroid hormone and increased metabolic rate. Causes include diffuse hyperplasia of the thyroid gland (Graves' disease), single nodule in the thyroid gland, and thyroiditis. The symptoms are related to the increased metabolic rate and include weight loss, fatigue, heat intolerance, excessive sweating, diarrhea, tachycardia, insomnia, muscle weakness, and tremor.

FULL_SYN

Overactive Thyroid

Has_NICHD_Parent

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C3009

label

Hyperthyroidism

Legacy_Concept_Name

Hyperthyroidism

NICHD_Hierarchy_Term

Hyperthyroidism

Preferred_Name

Hyperthyroidism

prefixIRI

C3123

prefLabel

Hyperthyroidism

Semantic_Type

Disease or Syndrome

UMLS_CUI

C0020550

subClassOf

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C27566

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C27565

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Delete Mapping To Ontology Source
http://purl.obolibrary.org/obo/HP_0000836 Human Phenotype Ontology LOOM
http://purl.bioontology.org/ontology/OMIM/MTHU001214 Online Mendelian Inheritance in Man LOOM
http://purl.bioontology.org/ontology/MESH/D006980 Medical Subject Headings LOOM
http://purl.bioontology.org/ontology/LNC/MTHU020782 Logical Observation Identifier Names and Codes LOOM
http://purl.obolibrary.org/obo/DOID_7998 Human Disease Ontology 123 LOOM