(Q5958740)

English

hyperthyroxinemia

thyroid disease

hyperthyroxinaemia

In more languages

Statements

0 references

class of disease

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thyroid gland disease

1 reference

Disease Ontology

30 November 2020

Disease Ontology ID

0 references

health specialty

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genetic association

1 reference

A point mutation in transthyretin increases affinity for thyroxine and produces euthyroid hyperthyroxinemia

on focus list of Wikimedia project

WikiProject Medicine

0 references

NCI Thesaurus ID

C131850

1 reference

Disease Ontology

15 May 2019

Disease Ontology ID

http://purl.obolibrary.org/obo/DOID_2855

1 reference

Disease Ontology

30 November 2020

Disease Ontology ID

http://identifiers.org/doid/DOID:2855

1 reference

Identifiers.org

https://registry.identifiers.org/registry/doid

Identifiers

MeSH descriptor ID

1 reference

Disease Ontology

15 May 2019

Disease Ontology ID

0 references

Disease Ontology ID

1 reference

Disease Ontology

30 November 2020

Disease Ontology ID

Experimental Factor Ontology ID

1 reference

based on heuristic

inferred by common DOID mappings on source and on Wikidata

Microsoft Academic ID

0 references

1 reference

imported from Wikimedia project

English Wikipedia

mapping relation type

0 references

1 reference

Disease Ontology

15 May 2019

Disease Ontology ID

WikiProjectMed ID

Hyperthyroxinemia

0 references

Sitelinks

Wikipedia(3 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

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