Oguchi disease-1 (Q7080278): Difference between revisions

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Updated Item
Removed claim: WikiProjectMed ID (P11143): Oguchi disease, дублирующееся значение / duplicate value
Tag: Manual revert
 
(42 intermediate revisions by 20 users not shown)
label / enlabel / en
Oguchi disease type 1
Oguchi disease-1
label / ttlabel / tt
 
Тумыштагы стационар төнге сукырлык
label / delabel / de
 
Oguchi-Syndrom
aliases / en / 0aliases / en / 0
Oguchi disease-1
description / ukdescription / uk
 
хвороба людини
description / hydescription / hy
 
մարդու հիվանդություն
Property / OMIM ID: 258100 / reference
 
stated in: Disease Ontology
retrieved: 28 August 2019
Timestamp+2019-08-28T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

Disease Ontology ID: DOID:0110712
Property / OMIM ID: 258100 / reference
stated in: Disease Ontology release 2018-07-05
retrieved: 11 July 2018
Timestamp+2018-07-11T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

Disease Ontology ID: DOID:0110712
 
Property / OMIM ID: 258100 / reference
 
stated in: Monarch Disease Ontology release 2018-06-29
retrieved: 6 August 2018
Timestamp+2018-08-06T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

Mondo ID: MONDO_0009775
Property / OMIM ID: 258100 / reference
stated in: Monarch Disease Ontology release 2018-06-29
retrieved: 6 August 2018
Timestamp+2018-08-06T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

Mondo ID: MONDO:0009775
 
Property / instance of
 
Property / instance of: disease / rank
Normal rank
 
Property / instance of: disease / reference
stated in: Disease Ontology release 2018-07-05
retrieved: 11 July 2018
Timestamp+2018-07-11T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

Disease Ontology ID: DOID:0110712
 
Property / Orphanet ID
 
Property / Orphanet ID: 75382 / rank
Normal rank
 
Property / Orphanet ID: 75382 / qualifier
 
Property / Orphanet ID: 75382 / reference
stated in: Monarch Disease Ontology release 2018-06-29
retrieved: 6 August 2018
Timestamp+2018-08-06T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

Mondo ID: MONDO:0009775
 
Property / subclass of: congenital stationary night blindness / reference
 
stated in: Disease Ontology
retrieved: 30 November 2020
Timestamp+2020-11-30T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

Disease Ontology ID: DOID:0110712
Property / subclass of
 
Property / subclass of: hereditary night blindness / rank
Normal rank
 
Property / subclass of: hereditary night blindness / reference
stated in: Disease Ontology release 2018-07-05
retrieved: 11 July 2018
Timestamp+2018-07-11T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

Disease Ontology ID: DOID:0110712
 
Property / exact match: http://purl.obolibrary.org/obo/DOID_0110712 / reference
 
stated in: Disease Ontology
retrieved: 30 November 2020
Timestamp+2020-11-30T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

Disease Ontology ID: DOID:0110712
Property / exact match: http://purl.obolibrary.org/obo/DOID_0110712 / reference
stated in: Disease Ontology release 2018-07-05
retrieved: 12 September 2018
Timestamp+2018-09-12T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

Disease Ontology ID: DOID:0110712
 
Property / exact match: http://identifiers.org/doid/DOID:0110712 / reference
 
stated in: Disease Ontology
retrieved: 10 July 2020
Timestamp+2020-07-10T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

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 / Disease Ontology ID: DOID:0110712 / reference
 
stated in: Disease Ontology
retrieved: 30 November 2020
Timestamp+2020-11-30T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

Disease Ontology ID: DOID:0110712
Property / Disease Ontology ID: DOID:0110712 / reference
stated in: Disease Ontology release 2018-07-05
retrieved: 11 July 2018
Timestamp+2018-07-11T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

Disease Ontology ID: DOID:0110712
 
Property / Disease Ontology ID
 
Property / Disease Ontology ID: DOID:0110712 / rank
Normal rank
 
Property / Disease Ontology ID: DOID:0110712 / qualifier
 
Property / Disease Ontology ID: DOID:0110712 / reference
stated in: Monarch Disease Ontology release 2018-06-29
retrieved: 6 August 2018
Timestamp+2018-08-06T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

Mondo ID: MONDO:0009775
 
Property / Mondo ID
 
Property / Mondo ID: MONDO:0009775 / rank
Normal rank
 
Property / Mondo ID: MONDO:0009775 / reference
stated in: Monarch Disease Ontology release 2018-06-29
retrieved: 6 August 2018
Timestamp+2018-08-06T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

Mondo ID: MONDO:0009775
 
Property / UMLS CUI: C1306122 / reference
 
stated in: Monarch Disease Ontology release 2018-06-29
retrieved: 6 August 2018
Timestamp+2018-08-06T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

Mondo ID: MONDO_0009775
Property / UMLS CUI: C1306122 / reference
stated in: Monarch Disease Ontology release 2018-06-29
retrieved: 6 August 2018
Timestamp+2018-08-06T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

Mondo ID: MONDO:0009775
 
Property / instance of
 
Property / instance of: rare disease / rank
 
Normal rank
Property / instance of
 
Property / instance of: class of disease / rank
 
Normal rank
Property / subclass of
 
Property / subclass of: genetic disease / rank
 
Normal rank
Property / subclass of: genetic disease / reference
 
stated in: Disease Ontology
retrieved: 15 May 2019
Timestamp+2019-05-15T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

Disease Ontology ID: DOID:0110712
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
Timestamp+2020-11-30T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

Disease Ontology ID: DOID:0110712
Property / exact match
 
Property / exact match: http://www.orpha.net/ORDO/Orphanet_75382 / rank
 
Normal rank
Property / genetic association
 
Property / genetic association: SAG / rank
 
Normal rank
Property / genetic association: SAG / reference
 
stated in: UniProt
UniProt protein ID: P10523
retrieved: 13 August 2019
Timestamp+2019-08-13T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0
Property / genetic association: SAG / reference
 
Property / Microsoft Academic ID
 
Property / Microsoft Academic ID: 2778310085 / rank
 
Normal rank
Property / on focus list of Wikimedia project
 
Property / on focus list of Wikimedia project: WikiProject Medicine / rank
 
Normal rank
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 / 0links / eswiki / badges / 0
 
links / ttwiki / namelinks / ttwiki / name
 
links / dewiki / namelinks / 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
  • CSNBO1
  • congenital stationary night blindness Oguchi type 1
  • Night Blindness, Congenital Stationary, Oguchi Type 1
  • Oguchi Disease type 1
  • OGUCHI DISEASE 1

Statements

Identifiers