Hexokinase deficiency (Q5749049): Difference between revisions

From Wikidata

Jump to navigation Jump to search

Browse history interactively

← Older editNewer edit →

Revision as of 14:42, 8 November 2023 (restore) TiagoLubianaBot (talk | contribs) Bots 792,850 edits ‎Updated Item: Fix formatting of MONDO ID ← Older edit		Revision as of 05:10, 17 November 2023 (restore) undo Renamerr (talk | contribs) 66,970,399 edits ‎Added [uk] description: медичний стан, batch #216864 Tag: quickstatements [2.0] Newer edit →
description / uk		description / uk
			медичний стан

---

Revision as of 05:10, 17 November 2023

medical condition

• Nonspherocytic hemolytic anemia due to hexokinase deficiency
• Hexokinase deficiency hemolytic anemia
• HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO HEXOKINASE DEFICIENCY

Language	Label	Description	Also known as
English	Hexokinase deficiency	medical condition	Nonspherocytic hemolytic anemia due to hexokinase deficiency Hexokinase deficiency hemolytic anemia HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO HEXOKINASE DEFICIENCY

Statements

instance of

class of disease

0 references

subclass of

hemolytic anemia due to a disorder of glycolytic enzymes

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

retrieved

28 July 2018

Mondo ID

MONDO:0009340

health specialty

hematology

0 references

genetic association

HK1

1 reference

stated in

Open Targets Platform

retrieved

24 August 2023

reference URL

https://platform.opentargets.org/evidence/ENSG00000156515/MONDO_0009340

based on heuristic

inferred from an Open Targets association score over 0.7

exact match

http://www.orpha.net/ORDO/Orphanet_90031

0 references

Identifiers

MeSH descriptor ID

C562995

mapping relation type

exact match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

retrieved

28 July 2018

Mondo ID

MONDO:0009340

GARD rare disease ID

3672

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

retrieved

28 July 2018

Mondo ID

MONDO:0009340

ICD-10 ID

D55.2

1 reference

imported from Wikimedia project

English Wikipedia

ICD-10-CM

D55.2

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

retrieved

28 July 2018

Mondo ID

MONDO:0009340

ICD-9 ID

282.3

1 reference

imported from Wikimedia project

English Wikipedia

Microsoft Academic ID

2779994328

0 references

Mondo ID

MONDO_0009340

0 references

OMIM ID

235700

mapping relation type

exact match

2 references

imported from Wikimedia project

English Wikipedia

stated in

Monarch Disease Ontology release 2018-06-29

retrieved

28 July 2018

Mondo ID

MONDO:0009340

Orphanet ID

90031

mapping relation type

exact match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

retrieved

28 July 2018

Mondo ID

MONDO:0009340

UMLS CUI

C3150343

mapping relation type

close match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

retrieved

28 July 2018

Mondo ID

MONDO:0009340

C0472792

mapping relation type

close match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

retrieved

28 July 2018

Mondo ID

MONDO:0009340

C3502059

1 reference

based on heuristic

inferred by common MeSH mappings on source and on Wikidata

stated in

UMLS 2023

retrieved

25 May 2023

C5681378

1 reference

based on heuristic

inferred by common Orphanet mappings on source and on Wikidata

stated in

UMLS 2023

retrieved

16 June 2023

UniProt disease ID

DI-01739

0 references

 

Sitelinks

Wikipedia(1 entry)

• enwiki Hexokinase deficiency

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)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q5749049&oldid=2012769722"