Hyperproinsulinemia (Q5958530)

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human disease

hyperproinsulinemia
HYPERPROINSULINEMIA

Language	Label	Description	Also known as
English	Hyperproinsulinemia	human disease	hyperproinsulinemia HYPERPROINSULINEMIA

Statements

0 references

1 reference

Familial hyperproinsulinemia. An autosomal dominant defect

genetic disease

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

0 references

genetic association

2 references

A structurally abnormal insulin causing human diabetes

Open Targets Platform

24 August 2023

https://platform.opentargets.org/evidence/ENSG00000254647/EFO_0009650

based on heuristic

inferred from an Open Targets association score over 0.7

250.80

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

Identifiers

MeSH descriptor ID

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

Experimental Factor Ontology ID

1 reference

based on heuristic

inferred by common MONDO mappings on source and on Wikidata

Microsoft Academic ID

0 references

0 references

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

0 references

Sitelinks

Wikipedia(2 entries)

enwiki Hyperproinsulinemia
ptwiki Hiperproinsulinemia

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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