(Q3043136)

English

enteropeptidase deficiency

human disease

ENTEROKINASE DEFICIENCY
Enteropeptidase Deficiency
Congenital enterokinase deficiency
enterokinase deficiency

In more languages

edit

Statements

0 references

0 references

congenital intestinal disease due to an enzymatic defect

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

28 July 2018

1 reference

30 November 2020

autosomal recessive disease

1 reference

30 November 2020

2 references

13 August 2019

Mutations in the proenteropeptidase gene are the molecular cause of congenital enteropeptidase deficiency

ICD-9-CM

277.89

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

28 July 2018

http://purl.obolibrary.org/obo/DOID_0111667

1 reference

30 November 2020

http://identifiers.org/doid/DOID:0111667

1 reference

stated in

Identifiers.org

reference URL

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

Identifiers

MeSH descriptor ID

C562649

mapping relation type

exact match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

28 July 2018

0 references

1 reference

30 November 2020

Google Knowledge Graph ID

0 references

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

0 references

mapping relation type

exact match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

28 July 2018

mapping relation type

exact match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

28 July 2018

mapping relation type

close match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

28 July 2018

0 references

Sitelinks

Wikipedia(1 entry)

frwiki Déficience en entérokinase

(Q3043136)

enteropeptidase deficiency

Statements

Identifiers

Sitelinks

Wikipedia(1 entry)

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)