Hexokinase deficiency (Q5749049): Difference between revisions
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Created claim: Property:P107, term (Q1969448) |
Changed reference of claim: subclass of (P279): hemolytic anemia due to a disorder of glycolytic enzymes (Q55789127), см. / see autofix на / on Property talk:P5270 |
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(36 intermediate revisions by 13 users not shown) | |||||||||||||||
label / fr | label / fr | ||||||||||||||
déficit en hexokinase | |||||||||||||||
aliases / en / 0 | aliases / en / 0 | ||||||||||||||
Nonspherocytic hemolytic anemia due to hexokinase deficiency | |||||||||||||||
aliases / en / 1 | aliases / en / 1 | ||||||||||||||
Hexokinase deficiency hemolytic anemia | |||||||||||||||
aliases / en / 2 | aliases / en / 2 | ||||||||||||||
HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO HEXOKINASE DEFICIENCY | |||||||||||||||
description / en | description / en | ||||||||||||||
medical condition | |||||||||||||||
description / uk | description / uk | ||||||||||||||
медичний стан | |||||||||||||||
Property / P107 (Deleted Property) | |||||||||||||||
Property / P107 (Deleted Property): term Property P107 not found, cannot determine the data type to use. / rank | |||||||||||||||
Property / OMIM ID | |||||||||||||||
Property / OMIM ID: 235700 / rank | |||||||||||||||
Normal rank | |||||||||||||||
Property / OMIM ID: 235700 / qualifier | |||||||||||||||
Property / OMIM ID: 235700 / reference | |||||||||||||||
Property / OMIM ID: 235700 / reference | |||||||||||||||
stated in: Monarch Disease Ontology release 2018-06-29 retrieved: 28 July 2018
Mondo ID: MONDO_0009340 | |||||||||||||||
Property / ICD-9 ID | |||||||||||||||
Property / ICD-9 ID: 282.3 / rank | |||||||||||||||
Normal rank | |||||||||||||||
Property / ICD-9 ID: 282.3 / reference | |||||||||||||||
Property / ICD-10 ID | |||||||||||||||
Property / ICD-10 ID: D55.2 / rank | |||||||||||||||
Normal rank | |||||||||||||||
Property / ICD-10 ID: D55.2 / reference | |||||||||||||||
Property / health specialty | |||||||||||||||
Property / health specialty: hematology / rank | |||||||||||||||
Normal rank | |||||||||||||||
Property / MeSH descriptor ID | |||||||||||||||
Property / MeSH descriptor ID: C562995 / rank | |||||||||||||||
Normal rank | |||||||||||||||
Property / MeSH descriptor ID: C562995 / qualifier | |||||||||||||||
Property / MeSH descriptor ID: C562995 / reference | |||||||||||||||
stated in: Monarch Disease Ontology release 2018-06-29 retrieved: 28 July 2018
Mondo ID: MONDO_0009340 | |||||||||||||||
Property / ICD-10-CM | |||||||||||||||
Property / ICD-10-CM: D55.2 / rank | |||||||||||||||
Normal rank | |||||||||||||||
Property / ICD-10-CM: D55.2 / reference | |||||||||||||||
stated in: Monarch Disease Ontology release 2018-06-29 retrieved: 28 July 2018
Mondo ID: MONDO_0009340 | |||||||||||||||
Property / GARD rare disease ID | |||||||||||||||
Property / GARD rare disease ID: 3672 / rank | |||||||||||||||
Normal rank | |||||||||||||||
Property / GARD rare disease ID: 3672 / reference | |||||||||||||||
stated in: Monarch Disease Ontology release 2018-06-29 retrieved: 28 July 2018
Mondo ID: MONDO_0009340 | |||||||||||||||
Property / UMLS CUI | |||||||||||||||
Property / UMLS CUI: C3150343 / rank | |||||||||||||||
Normal rank | |||||||||||||||
Property / UMLS CUI: C3150343 / qualifier | |||||||||||||||
Property / UMLS CUI: C3150343 / reference | |||||||||||||||
stated in: Monarch Disease Ontology release 2018-06-29 retrieved: 28 July 2018
Mondo ID: MONDO_0009340 | |||||||||||||||
Property / UMLS CUI | |||||||||||||||
Property / UMLS CUI: C0472792 / rank | |||||||||||||||
Normal rank | |||||||||||||||
Property / UMLS CUI: C0472792 / qualifier | |||||||||||||||
Property / UMLS CUI: C0472792 / reference | |||||||||||||||
stated in: Monarch Disease Ontology release 2018-06-29 retrieved: 28 July 2018
Mondo ID: MONDO_0009340 | |||||||||||||||
Property / UMLS CUI | |||||||||||||||
Property / UMLS CUI: C3502059 / rank | |||||||||||||||
Normal rank | |||||||||||||||
Property / UMLS CUI: C3502059 / reference | |||||||||||||||
based on heuristic: inferred by common MeSH mappings on source and on Wikidata stated in: UMLS 2023 retrieved: 25 May 2023
| |||||||||||||||
Property / UMLS CUI | |||||||||||||||
Property / UMLS CUI: C5681378 / rank | |||||||||||||||
Normal rank | |||||||||||||||
Property / UMLS CUI: C5681378 / reference | |||||||||||||||
based on heuristic: inferred by common Orphanet mappings on source and on Wikidata stated in: UMLS 2023 retrieved: 16 June 2023
| |||||||||||||||
Property / Orphanet ID | |||||||||||||||
Property / Orphanet ID: 90031 / rank | |||||||||||||||
Normal rank | |||||||||||||||
Property / Orphanet ID: 90031 / qualifier | |||||||||||||||
Property / Orphanet ID: 90031 / reference | |||||||||||||||
stated in: Monarch Disease Ontology release 2018-06-29 retrieved: 28 July 2018
Mondo ID: MONDO_0009340 | |||||||||||||||
Property / subclass of | |||||||||||||||
Property / subclass of: hemolytic anemia due to a disorder of glycolytic enzymes / rank | |||||||||||||||
Normal rank | |||||||||||||||
Property / subclass of: hemolytic anemia due to a disorder of glycolytic enzymes / reference | |||||||||||||||
stated in: Monarch Disease Ontology release 2018-06-29 retrieved: 28 July 2018
Mondo ID: MONDO_0009340 | |||||||||||||||
Property / exact match | |||||||||||||||
Property / exact match: http://www.orpha.net/ORDO/Orphanet_90031 / rank | |||||||||||||||
Normal rank | |||||||||||||||
Property / Microsoft Academic ID | |||||||||||||||
Property / Microsoft Academic ID: 2779994328 / rank | |||||||||||||||
Normal rank | |||||||||||||||
Property / instance of | |||||||||||||||
Property / instance of: class of disease / rank | |||||||||||||||
Normal rank | |||||||||||||||
Property / genetic association | |||||||||||||||
Property / genetic association: HK1 / rank | |||||||||||||||
Normal rank | |||||||||||||||
Property / genetic association: HK1 / 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 | |||||||||||||||
Property / UniProt disease ID | |||||||||||||||
Property / UniProt disease ID: DI-01739 / rank | |||||||||||||||
Normal rank | |||||||||||||||
Property / Mondo ID | |||||||||||||||
Property / Mondo ID: MONDO_0009340 / rank | |||||||||||||||
Normal rank |
Latest revision as of 20:02, 25 February 2024
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 |
|
Statements
Identifiers
1 reference
1 reference
1 reference
1 reference
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1 reference
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Sitelinks
Wikipedia(1 entry)
- enwiki Hexokinase deficiency