Oguchi disease-1 (Q7080278): Difference between revisions
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Removed claim: WikiProjectMed ID (P11143): Oguchi disease, дублирующееся значение / duplicate value Tag: Manual revert |
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label / tt | label / tt | ||||||||||||||
Тумыштагы стационар төнге сукырлык | |||||||||||||||
label / de | label / de | ||||||||||||||
Oguchi-Syndrom | |||||||||||||||
aliases / en / 0 | aliases / en / 0 | ||||||||||||||
description / uk | description / uk | ||||||||||||||
хвороба людини | |||||||||||||||
description / hy | description / hy | ||||||||||||||
մարդու հիվանդություն | |||||||||||||||
Property / OMIM ID: 258100 / reference | |||||||||||||||
stated in: Disease Ontology retrieved: 28 August 2019
Disease Ontology ID: DOID:0110712 | |||||||||||||||
Property / OMIM ID: 258100 / reference | |||||||||||||||
retrieved: 28 August 2019
Disease Ontology ID: DOID:0110712 | |||||||||||||||
Property / OMIM ID: 258100 / reference | |||||||||||||||
stated in: Monarch Disease Ontology release 2018-06-29 retrieved: 6 August 2018
Mondo ID: MONDO_0009775 | |||||||||||||||
Property / OMIM ID: 258100 / reference | |||||||||||||||
retrieved: 6 August 2018
Mondo ID: MONDO:0009775 | |||||||||||||||
Property / instance of | |||||||||||||||
Property / instance of: disease / rank | |||||||||||||||
Property / instance of: disease / reference | |||||||||||||||
retrieved: 15 May 2019
Disease Ontology ID: DOID:0110712 | |||||||||||||||
Property / Orphanet ID | |||||||||||||||
Property / Orphanet ID: 75382 / rank | |||||||||||||||
Property / Orphanet ID: 75382 / qualifier | |||||||||||||||
Property / Orphanet ID: 75382 / reference | |||||||||||||||
retrieved: 6 August 2018
Mondo ID: MONDO:0009775 | |||||||||||||||
Property / subclass of: congenital stationary night blindness / reference | |||||||||||||||
stated in: Disease Ontology retrieved: 30 November 2020
Disease Ontology ID: DOID:0110712 | |||||||||||||||
Property / subclass of: congenital stationary night blindness / reference | |||||||||||||||
retrieved: 15 May 2019
Disease Ontology ID: DOID:0110712 | |||||||||||||||
Property / subclass of: genetic disease / reference | |||||||||||||||
stated in: Disease Ontology retrieved: 15 May 2019
Disease Ontology ID: DOID:0110712 | |||||||||||||||
Property / subclass of: genetic disease / reference | |||||||||||||||
retrieved: 15 May 2019
Disease Ontology ID: DOID:0110712 | |||||||||||||||
Property / exact match: http://purl.obolibrary.org/obo/DOID_0110712 / reference | |||||||||||||||
stated in: Disease Ontology retrieved: 30 November 2020
Disease Ontology ID: DOID:0110712 | |||||||||||||||
Property / exact match: http://purl.obolibrary.org/obo/DOID_0110712 / reference | |||||||||||||||
retrieved: 28 August 2019
Disease Ontology ID: DOID:0110712 | |||||||||||||||
Property / exact match: http://purl.obolibrary.org/obo/DOID_0110712 / reference | |||||||||||||||
retrieved: 10 July 2020
Disease Ontology ID: DOID:0110712 | |||||||||||||||
Property / exact match: http://identifiers.org/doid/DOID:0110712 / reference | |||||||||||||||
stated in: Disease Ontology retrieved: 10 July 2020
Disease Ontology ID: DOID:0110712 | |||||||||||||||
Property / exact match: http://identifiers.org/doid/DOID:0110712 / reference | |||||||||||||||
Property / exact match: http://identifiers.org/doid/DOID:0110712 / reference | |||||||||||||||
Property / exact match: http://identifiers.org/doid/DOID:0110712 / reference | |||||||||||||||
retrieved: 10 July 2020
Disease Ontology ID: DOID:0110712 | |||||||||||||||
Property / Disease Ontology ID: DOID:0110712 / reference | |||||||||||||||
stated in: Disease Ontology retrieved: 30 November 2020
Disease Ontology ID: DOID:0110712 | |||||||||||||||
Property / Disease Ontology ID: DOID:0110712 / reference | |||||||||||||||
retrieved: 28 August 2019
Disease Ontology ID: DOID:0110712 | |||||||||||||||
Property / Disease Ontology ID: DOID:0110712 / reference | |||||||||||||||
retrieved: 10 July 2020
Disease Ontology ID: DOID:0110712 | |||||||||||||||
Property / Disease Ontology ID | |||||||||||||||
Property / Disease Ontology ID: DOID:0110712 / rank | |||||||||||||||
Property / Disease Ontology ID: DOID:0110712 / qualifier | |||||||||||||||
Property / Disease Ontology ID: DOID:0110712 / reference | |||||||||||||||
retrieved: 6 August 2018
Mondo ID: MONDO:0009775 | |||||||||||||||
Property / Mondo ID | |||||||||||||||
Property / Mondo ID: MONDO:0009775 / rank | |||||||||||||||
Property / Mondo ID: MONDO:0009775 / reference | |||||||||||||||
retrieved: 6 August 2018
Mondo ID: MONDO:0009775 | |||||||||||||||
Property / UMLS CUI: C1306122 / reference | |||||||||||||||
stated in: Monarch Disease Ontology release 2018-06-29 retrieved: 6 August 2018
Mondo ID: MONDO_0009775 | |||||||||||||||
Property / UMLS CUI: C1306122 / reference | |||||||||||||||
retrieved: 6 August 2018
Mondo ID: MONDO:0009775 | |||||||||||||||
Property / instance of | |||||||||||||||
Property / instance of: class of disease / rank | |||||||||||||||
Normal rank | |||||||||||||||
Property / subclass of | |||||||||||||||
Property / subclass of: autosomal recessive disease / rank | |||||||||||||||
Normal rank | |||||||||||||||
Property / subclass of: autosomal recessive disease / reference | |||||||||||||||
stated in: Disease Ontology retrieved: 30 November 2020
Disease Ontology ID: DOID:0110712 | |||||||||||||||
Property / ICD-11 ID (Foundation) | |||||||||||||||
Property / ICD-11 ID (Foundation): 1759055065 / rank | |||||||||||||||
Normal rank | |||||||||||||||
Property / UniProt disease ID | |||||||||||||||
Property / UniProt disease ID: DI-00374 / rank | |||||||||||||||
Normal rank | |||||||||||||||
Property / WikiProjectMed ID | |||||||||||||||
Property / WikiProjectMed ID: Oguchi disease / rank | |||||||||||||||
Normal rank | |||||||||||||||
Property / Mondo ID | |||||||||||||||
Property / Mondo ID: MONDO_0009775 / rank | |||||||||||||||
Normal rank | |||||||||||||||
links / eswiki / badges / 0 | links / eswiki / badges / 0 | ||||||||||||||
links / ttwiki / name | links / ttwiki / name | ||||||||||||||
links / dewiki / name | links / dewiki / name | ||||||||||||||
Latest revision as of 08:29, 15 June 2024
human disease
- CSNBO1
- congenital stationary night blindness Oguchi type 1
- Night Blindness, Congenital Stationary, Oguchi Type 1
- Oguchi Disease type 1
- OGUCHI DISEASE 1
Language | Label | Description | Also known as |
---|---|---|---|
English | Oguchi disease-1 |
human disease |
|
Statements
1 reference
1 reference
1 reference
1 reference
Identifiers
1 reference
1 reference
1 reference
1 reference
Sitelinks
Wikipedia(6 entries)
- dewiki Oguchi-Syndrom
- enwiki Oguchi disease
- eswiki Enfermedad de Oguchi
- plwiki Choroba Oguchiego
- ruwiki Болезнь Огучи
- ttwiki Тумыштагы стационар төнге сукырлык