Horner's syndrome (Q1126839): Difference between revisions

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Egon Willighagen (talk | contribs)
Created claim: OpenAlex ID (P10283): C2776252412, batch #74564
Nataev (talk | contribs)
Page on [uzwiki] deleted: Gorner sindromi
Tag: Automatic update from connected wiki
 
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label / idlabel / id
 
Sindrom Horner
label / uzlabel / uz
 
Gorner sindromi
label / sllabel / sl
 
Hornerjev sindrom
label / eolabel / eo
 
sindromo de Horner
aliases / ca / 0aliases / ca / 0
 
síndrome de Horner
aliases / ca / 1aliases / ca / 1
síndrome de Bernard
aliases / nb / 0aliases / nb / 0
 
okulosympatisk parese
aliases / zh-hant / 0aliases / zh-hant / 0
 
霍纳氏症候群
description / endescription / en
A disease characterized by miosis (a constricted pupil), partial ptosis (a weak, droopy eyelid), apparent anhydrosis (decreased sweating), with apparent enophthalmos (inset eyeball)
disease characterized by miosis (a constricted pupil), partial ptosis (a weak, droopy eyelid), apparent anhydrosis (decreased sweating), with apparent enophthalmos (inset eyeball)
description / nbdescription / nb
 
en øyelidelse
description / sldescription / sl
 
bolezen, za katero so značilni mioza (zožena zenica), delna ptoza (šibka, povešena veka) in vidna anhidroza (zmanjšano znojenje) z enoftalmusom (vdrto očesno zrklo)
description / ukdescription / uk
 
хвороба
Property / Encyclopædia Britannica Online ID: science/Horners-syndrome / qualifier
 
subject named as: Horner’s syndrome
Property / ICD-10-CM: G90.2 / reference
 
stated in: Monarch Disease Ontology release 2018-06-29
retrieved: 27 July 2018
Timestamp+2018-07-27T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

Mondo ID: MONDO_0001294
Property / ICD-10-CM: G90.2 / reference
stated in: Monarch Disease Ontology release 2018-06-29
retrieved: 27 July 2018
Timestamp+2018-07-27T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

Mondo ID: MONDO:0001294
 
Property / GARD rare disease ID: 6670 / reference
 
stated in: Monarch Disease Ontology release 2018-06-29
retrieved: 27 July 2018
Timestamp+2018-07-27T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

Mondo ID: MONDO_0001294
Property / GARD rare disease ID: 6670 / reference
stated in: Monarch Disease Ontology release 2018-06-29
retrieved: 27 July 2018
Timestamp+2018-07-27T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

Mondo ID: MONDO:0001294
 
Property / MeSH descriptor ID: D006732 / qualifier
 
subject named as: Horner Syndrome
Property / MeSH descriptor ID: D006732 / reference
 
stated in: Monarch Disease Ontology release 2018-06-29
retrieved: 27 July 2018
Timestamp+2018-07-27T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

Mondo ID: MONDO_0001294
Property / MeSH descriptor ID: D006732 / reference
stated in: Monarch Disease Ontology release 2018-06-29
retrieved: 27 July 2018
Timestamp+2018-07-27T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

Mondo ID: MONDO:0001294
 
Property / ICD-9-CM: 337.09 / reference
 
stated in: Monarch Disease Ontology release 2018-06-29
retrieved: 27 July 2018
Timestamp+2018-07-27T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

Mondo ID: MONDO_0001294
Property / ICD-9-CM: 337.09 / reference
stated in: Monarch Disease Ontology release 2018-06-29
retrieved: 27 July 2018
Timestamp+2018-07-27T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

Mondo ID: MONDO:0001294
 
Property / Mondo ID
 
Property / Mondo ID: MONDO:0001294 / rank
Normal rank
 
Property / Mondo ID: MONDO:0001294 / reference
stated in: Monarch Disease Ontology release 2018-06-29
retrieved: 27 July 2018
Timestamp+2018-07-27T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

Mondo ID: MONDO:0001294
 
Property / OpenAlex ID: C2776252412 / reference
 
stated in: OpenAlex
retrieved: 26 January 2022
Timestamp+2022-01-26T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

reference URL: https://docs.openalex.org/download-snapshot/snapshot-data-format
archive URL: https://web.archive.org/web/20220125070108/https://docs.openalex.org/download-snapshot/snapshot-data-format
archive date: 25 January 2022
Timestamp+2022-01-25T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0
Property / subclass of
 
Property / subclass of: disease / rank
 
Normal rank
Property / MeSH tree code
 
Property / MeSH tree code: C10.228.140.232.750 / rank
 
Normal rank
Property / instance of
 
Property / instance of: class of disease / rank
 
Normal rank
Property / PatientsLikeMe condition ID
 
Property / PatientsLikeMe condition ID: horner-s-syndrome / rank
 
Normal rank
Property / WikiProjectMed ID
 
Property / WikiProjectMed ID: Horner's syndrome / rank
 
Normal rank
Property / Mondo ID
 
Property / Mondo ID: MONDO_0001294 / rank
 
Normal rank
links / eswiki / namelinks / eswiki / name
links / idwiki / namelinks / idwiki / name
 

Latest revision as of 17:25, 17 October 2024

disease characterized by miosis (a constricted pupil), partial ptosis (a weak, droopy eyelid), apparent anhydrosis (decreased sweating), with apparent enophthalmos (inset eyeball)
  • Bernard Horner syndrome
  • Horner syndrome
  • cervical sympathetic paralysis
  • Oculosympathetic Palsy
  • Bernard-Horner Syndrome
Language Label Description Also known as
English
Horner's syndrome
disease characterized by miosis (a constricted pupil), partial ptosis (a weak, droopy eyelid), apparent anhydrosis (decreased sweating), with apparent enophthalmos (inset eyeball)
  • Bernard Horner syndrome
  • Horner syndrome
  • cervical sympathetic paralysis
  • Oculosympathetic Palsy
  • Bernard-Horner Syndrome

Statements

Identifiers

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8D8A.1
Horner syndrome
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