Congenital hypopituitarism (Q5160439)

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human disease

• Congenital combined pituitary hormone deficiency

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Language	Label	Description	Also known as
English	Congenital hypopituitarism	human disease	Congenital combined pituitary hormone deficiency

Statements

instance of

class of disease

0 references

subclass of

hypopituitarism

0 references

non-acquired pituitary hormone deficiency

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

retrieved

28 July 2018

Mondo ID

MONDO_0018762

exact match

http://www.orpha.net/ORDO/Orphanet_467

0 references

Identifiers

GARD rare disease ID

2252

0 references

ICD-10 ID

Q89.2

1 reference

imported from Wikimedia project

English Wikipedia

ICD-10-CM

E23.0

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

retrieved

28 July 2018

Mondo ID

MONDO_0018762

ICD-9 ID

759.2

1 reference

imported from Wikimedia project

English Wikipedia

Mondo ID

MONDO_0018762

0 references

OMIM ID

275200

1 reference

imported from Wikimedia project

English Wikipedia

Orphanet ID

467

mapping relation type

exact match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

retrieved

28 July 2018

Mondo ID

MONDO_0018762

UMLS CUI

C5680091

1 reference

based on heuristic

inferred by common Orphanet mappings on source and on Wikidata

stated in

UMLS 2023

retrieved

16 June 2023

 

Sitelinks

Wikipedia(1 entry)

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• enwiki Congenital hypopituitarism

Wikibooks(0 entries)

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Wikinews(0 entries)

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Wikiquote(0 entries)

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Wikisource(0 entries)

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Wikiversity(0 entries)

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Wikivoyage(0 entries)

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Wiktionary(0 entries)

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Multilingual sites(0 entries)

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