(Q5432934)

English

familial dysalbuminemic hyperthyroxinemia

medical condition

FDAH
HYPERTHYROXINEMIA, FAMILIAL DYSALBUMINEMIC; FDAH
HYPERTHYROXINEMIA, FAMILIAL DYSALBUMINEMIC
Fdh
Euthyroid Hyperthyroxinemia 1

In more languages

Statements

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class of disease

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hyperthyroxinemia

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genetic disease

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

health specialty

1 reference

Medical Subject Headings

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Medical Subject Headings

genetic association

1 reference

A point mutation in the human serum albumin gene results in familial dysalbuminaemic hyperthyroxinaemia

http://www.orpha.net/ORDO/Orphanet_276271

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Identifiers

MeSH descriptor ID

mapping relation type

2 references

imported from Wikimedia project

English Wikipedia

Monarch Disease Ontology release 2018-06-29

28 July 2018

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C19.874.410.249

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1 reference

imported from Wikimedia project

English Wikipedia

Microsoft Academic ID

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1 reference

imported from Wikimedia project

English Wikipedia

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

UniProt disease ID

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WikiProjectMed ID

Familial dysalbuminemic hyperthyroxinemia

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Sitelinks

Wikipedia(2 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

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Wiktionary(0 entries)

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