Movatterモバイル変換
[0]
ホーム
URL:
画像なし
夜間モード
Jump to content
Main menu
Main menu
move to sidebar
hide
Navigation
Main page
Community portal
Project chat
Create a new Item
Recent changes
Random Item
Query Service
Nearby
Help
Special pages
Lexicographical data
Create a new Lexeme
Recent changes
Random Lexeme
Search
Search
English
Appearance
Donate
Create account
Log in
Personal tools
Donate
Create account
Log in
cystic fibrosis
(Q178194)
Item
Discussion
English
Read
View history
Tools
Tools
move to sidebar
hide
Actions
Read
View history
General
What links here
Related changes
Permanent link
Page information
Cite this page
Get shortened URL
Download QR code
Concept URI
Print/export
Create a book
Download as PDF
Printable version
In other projects
Appearance
move to sidebar
hide
From Wikidata
autosomal recessive disease characterized by the buildup of mucus
CF
mucoviscidosis
CYSTIC FIBROSIS
CYSTIC FIBROSIS; CF
edit
Language
Label
Description
Also known as
default for all languages
No label defined
–
English
cystic fibrosis
autosomal recessive disease characterized by the buildup of mucus
CF
mucoviscidosis
CYSTIC FIBROSIS
CYSTIC FIBROSIS; CF
Statements
instance of
designated intractable/rare disease
1 reference
reference URL
https://ddrare.nibiohn.go.jp/
retrieved
17 May 2019
class of disease
0 references
symptom or sign
0 references
subclass of
autosomal recessive disease
2 references
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0009061
stated in
Disease Ontology
retrieved
29 November 2020
Disease Ontology ID
DOID:1485
lung disease
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0009061
genetic biliary tract disease
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0009061
genetic pancreatic disease
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0009061
rare genetic respiratory disease
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0009061
rare male fertility disorder with obstructive azoospermia
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0009061
rare genetic disorder with obstructive azoospermia
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0009061
syndrome
1 reference
stated in
Disease Ontology
retrieved
29 November 2020
Disease Ontology ID
DOID:1485
disease
0 references
image
ClubbingCF.JPG
2,331 × 1,743; 372 KB
media legend
Clubbing in the fingers of a person with cystic fibrosis
(English)
0 references
health specialty
medical genetics
1 reference
imported from Wikimedia project
English Wikipedia
pediatrics
0 references
pulmonology
0 references
symptoms and signs
bowel obstruction
0 references
osteoporosis
0 references
peptic ulcer disease
0 references
cholestasis
0 references
hepatitis
0 references
gallstone
0 references
liver cirrhosis
0 references
bronchitis
0 references
pneumonia
0 references
atelectasis
0 references
bronchiectasis
0 references
pulmonary fibrosis
0 references
muscle weakness
0 references
dyspnea
0 references
cyanosis
0 references
heart failure
0 references
medical examination
physical examination
0 references
Sweat test
0 references
screening
class of object(s) of occurrence
sweat
meconium
0 references
drug or therapy used for treatment
sodium phenylbutyrate
1 reference
stated in
NDF-RT
NDF-RT ID
N0000148497
language of work or name
English
retrieved
13 December 2016
dornase alfa
2 references
stated in
NDF-RT
NDF-RT ID
N0000148342
language of work or name
English
retrieved
13 December 2016
stated in
Drug Indications Extracted from FAERS
retrieved
2 October 2018
amiloride
1 reference
stated in
NDF-RT
NDF-RT ID
N0000147699
language of work or name
English
retrieved
13 December 2016
N-acetyl-L-cysteine
1 reference
stated in
NDF-RT
NDF-RT ID
N0000147113
language of work or name
English
retrieved
13 December 2016
ivacaftor
1 reference
stated in
Drug Indications Extracted from FAERS
retrieved
2 October 2018
tobramycin
1 reference
stated in
Drug Indications Extracted from FAERS
retrieved
2 October 2018
aztreonam
1 reference
stated in
Drug Indications Extracted from FAERS
retrieved
2 October 2018
tobramycin
start time
12 February 2014
approved by
Food and Drug Administration
1 reference
stated in
Inxight: Drugs Database
retrieved
2 November 2018
reference URL
https://drugs.ncats.io/drug/VZ8RRZ51VK
elexacaftor/ivacaftor/tezacaftor
0 references
genetic association
AGTR2
determination method or standard
genome-wide association study
TAS
1 reference
reference URL
https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_1485&ncbiId=186
http://www.genome.gov/gwastudies/index.cfm?gene=AGTR2
stated in
Phenocarta
Genome-wide association and linkage identify modifier loci of lung disease severity in cystic fibrosis at 11p13 and 20q13.2.
retrieved
25 May 2020
SLC8A3
determination method or standard
genome-wide association study
TAS
1 reference
reference URL
https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_1485&ncbiId=6547
http://www.genome.gov/gwastudies/index.cfm?gene=SLC8A3
stated in
Phenocarta
Genome-wide association and linkage identify modifier loci of lung disease severity in cystic fibrosis at 11p13 and 20q13.2.
retrieved
25 May 2020
AHRR
determination method or standard
genome-wide association study
TAS
1 reference
reference URL
https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_1485&ncbiId=57491
http://www.genome.gov/gwastudies/index.cfm?gene=AHRR
stated in
Phenocarta
Genome-wide association and linkage identify modifier loci of lung disease severity in cystic fibrosis at 11p13 and 20q13.2.
retrieved
25 May 2020
CFTR
2 references
stated in
UniProt
UniProt protein ID
P13569
retrieved
13 August 2019
stated in
Open Targets Platform
retrieved
24 August 2023
reference URL
https://platform.opentargets.org/evidence/ENSG00000001626/MONDO_0009061
based on heuristic
inferred from an Open Targets association score over 0.7
external data available at URL
http://www.nanbyou.or.jp/entry/4531
language of work or name
Japanese
1 reference
reference URL
https://ddrare.nibiohn.go.jp/
retrieved
17 May 2019
on focus list of Wikimedia project
WikiProject Medicine
0 references
ICD-9-CM
277.0
2 references
stated in
Disease Ontology
retrieved
15 May 2019
Disease Ontology ID
DOID:1485
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0009061
ICPC 2 ID
T99
1 reference
imported from Wikimedia project
Spanish Wikipedia
NCI Thesaurus ID
C2975
1 reference
stated in
Disease Ontology
retrieved
15 May 2019
Disease Ontology ID
DOID:1485
exact match
http://purl.obolibrary.org/obo/DOID_1485
1 reference
stated in
Disease Ontology
retrieved
29 November 2020
Disease Ontology ID
DOID:1485
http://identifiers.org/doid/DOID:1485
1 reference
stated in
Identifiers.org
reference URL
https://registry.identifiers.org/registry/doid
http://www.orpha.net/ORDO/Orphanet_586
0 references
Commons category
Cystic fibrosis
0 references
topic's main category
Category:Cystic fibrosis
0 references
Identifiers
National Library of Spain SpMaBN ID (BNE v1.0)
XX534572
0 references
Bibliothèque nationale de France ID
11956777v
1 reference
stated in
Integrated Authority File
GND ID
4040669-6
1 reference
imported from Wikimedia project
German Wikipedia
National Library of Israel J9U ID
987007538476705171
1 reference
stated in
National Library of Israel
Library of Congress authority ID
sh85035204
1 reference
stated in
Integrated Authority File
National Library of Latvia ID
000115516
0 references
NDL Authority ID
00570677
0 references
NL CR AUT ID
ph119277
subject named as
cystická fibróza
0 references
Dewey Decimal Classification
616.24
1 reference
stated in
Integrated Authority File
616.372
1 reference
stated in
Integrated Authority File
618.92372
1 reference
stated in
Integrated Authority File
618.9224
1 reference
stated in
Integrated Authority File
Library of Congress Classification
RC858.C95
1 reference
stated in
Library of Congress Name Authority File
MeSH descriptor ID
D003550
mapping relation type
exact match
subject named as
Cystic Fibrosis
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0009061
MeSH tree code
C06.689.202
broader concept
pancreas disease
0 references
C08.381.187
broader concept
lung disease
0 references
C16.320.190
broader concept
genetic disease
0 references
C16.614.213
broader concept
perinatal disease
0 references
MedlinePlus ID
000107
1 reference
imported from Wikimedia project
English Wikipedia
PatientsLikeMe condition ID
cystic-fibrosis
0 references
KEGG ID
H00218
0 references
Australian Educational Vocabulary ID
scot/16747
0 references
BBC News topic ID
c207p54ml5gt
0 references
BBC Things ID
53613dfc-58c9-4e1e-9151-182db224111f
1 reference
stated in
BBC Things
BNCF Thesaurus ID
20386
1 reference
stated in
Nuovo soggettario
Brockhaus Enzyklopädie online ID
zystische-fibrose
0 references
Cultureel Woordenboek ID
levenswetenschappen-en-geneeskunde/cystische-fibrose
0 references
Disease Ontology ID
DOID:1485
1 reference
stated in
Disease Ontology
retrieved
29 November 2020
Disease Ontology ID
DOID:1485
DiseasesDB
3347
1 reference
imported from Wikimedia project
English Wikipedia
Elhuyar ZTH ID
028445
0 references
eMedicine ID
1001602
1 reference
imported from Wikimedia project
English Wikipedia
Encyclopædia Britannica Online ID
science/cystic-fibrosis
subject named as
cystic fibrosis
0 references
Encyclopædia Universalis ID
mucoviscidose-fibrose-kystique-du-pancreas
0 references
Encyclopedia of China (Third Edition) ID
448509
0 references
Freebase ID
/m/0dcp_
1 reference
stated in
Freebase Data Dumps
publication date
28 October 2013
GARD rare disease ID
6233
2 references
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0009061
stated in
Disease Ontology
retrieved
15 May 2019
Disease Ontology ID
DOID:1485
GeneReviews ID
NBK1250
0 references
Genetics Home Reference Conditions ID
cystic-fibrosis
0 references
Golden ID
Cystic_fibrosis-X9MMB
0 references
Gran Enciclopèdia Catalana ID
mucoviscidosi
0 references
Gran Enciclopèdia Catalana ID (former scheme)
0125099
0 references
Hrvatska enciklopedija ID
11965
0 references
ICD-10 ID
E84
0 references
ICD-10-CM
E84.9
2 references
stated in
Disease Ontology
retrieved
15 May 2019
Disease Ontology ID
DOID:1485
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0009061
E84
2 references
stated in
Disease Ontology
retrieved
15 May 2019
Disease Ontology ID
DOID:1485
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0009061
E84.0
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0009061
E84.1
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0009061
E84.8
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0009061
ICD-11 ID (Foundation)
514403112
0 references
ICD-11 ID (MMS)
CA25
subject named as
Cystic fibrosis
0 references
JSTOR topic ID (archived)
cystic-fibrosis
0 references
KBpedia ID
CysticFibrosis
1 reference
stated in
KBpedia
retrieved
9 July 2020
LEM ID
LEM201003805
0 references
Lex ID
cystisk_fibrose
0 references
Medical Dictionary for Regulatory Activities ID
10011762
1 reference
reference URL
https://cdn.who.int/media/docs/default-source/classification/icd/icd-10/icd-10-to-meddra-map---june-2023---codes-mapping.xlsx
based on heuristic
inferred by common ICD-10 mappings on Wikidata and on source
Microsoft Academic ID
2910021119
0 references
2910515979
0 references
Mondo ID
MONDO_0009061
0 references
NALT ID
31334
0 references
NE.se ID
cystisk-fibros
0 references
NHS Health A to Z ID
cystic-fibrosis
0 references
OmegaWiki Defined Meaning
1311566
0 references
OMIM ID
219700
1 reference
stated in
Disease Ontology
retrieved
15 May 2019
Disease Ontology ID
DOID:1485
OpenAlex ID
C2776938444
1 reference
stated in
OpenAlex
retrieved
26 January 2022
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
Orphanet ID
586
mapping relation type
exact match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0009061
Patientplus ID
cystic-fibrosis-pro
1 reference
reference URL
http://www.patient.co.uk/patientplus/c.htm
Quora topic ID
Cystic-Fibrosis
1 reference
stated in
Quora
SNOMED CT ID
190905008
0 references
Store medisinske leksikon ID
cystisk_fibrose
mapping relation type
exact match
subject named as
cystisk fibrose
1 reference
stated in
Great Norwegian Encyclopedia
retrieved
16 March 2020
subreddit
CysticFibrosis
subject named as
Cystic Fibrosis
start time
27 September 2009
language of work or name
English
point in time
23 May 2023
0 references
UK Archival Thesaurus ID
f2/mt285/649/3032/8690/8012/7939
subject named as
Cystic fibrosis
0 references
UK Parliament thesaurus ID
9540
subject named as
Cystic fibrosis
0 references
UMLS CUI
C0010674
1 reference
stated in
Disease Ontology
retrieved
15 May 2019
Disease Ontology ID
DOID:1485
C1527396
1 reference
stated in
WikiUMLS: Aligning UMLS to Wikipedia via Cross-lingual Neural Ranking
C0392164
1 reference
based on heuristic
inferred by common MeSH mappings on source and on Wikidata
stated in
UMLS 2023
retrieved
25 May 2023
UniProt disease ID
DI-01466
0 references
Vikidia article ID
fr:Mucoviscidose
0 references
WikiKids ID
Taaislijmziekte
0 references
WikiProjectMed ID
Cystic fibrosis
0 references
WikiSkripta article ID
1329
0 references
Wolfram Language entity code
Entity["Disease", "ICDNine277.0"]
0 references
Entity["Disease", {"ICDNine277.0", "Primary"}]
0 references
WordNet 3.1 Synset ID
14178988-n
0 references
Yale LUX ID
concept/9d51b2b3-e319-448b-a5cd-1437ddaf1dfa
0 references
YSO ID
26696
1 reference
stated in
YSO-Wikidata mapping project
Sitelinks
Wikipedia
(64 entries)
edit
afwiki
Sistiese fibrose
arwiki
تليف كيسي
astwiki
Fibrosis quística
azbwiki
کیستیک فیبروزیس
azwiki
Sistik fibroz
bswiki
Cistična fibroza
cawiki
Fibrosi quística
ckbwiki
سیستیک فایبرۆسس
cswiki
Cystická fibróza
cywiki
Ffibrosis systig
dawiki
Cystisk fibrose
dewiki
Mukoviszidose
elwiki
Κυστική ίνωση
enwiki
Cystic fibrosis
eowiki
Mukoviskozeco
eswiki
Fibrosis quística
etwiki
Tsüstiline fibroos
euwiki
Fibrosi kistiko
fawiki
فیبروز سیستیک
fiwiki
Kystinen fibroosi
frwiki
Mucoviscidose
gawiki
Fiobróis chisteach
glwiki
Fibrose quística
hewiki
סיסטיק פיברוזיס
hiwiki
सिस्टिक फाइब्रोसिस
huwiki
Cisztás fibrózis
hywiki
Ցիստիկ ֆիբրոզ
idwiki
Fibrosis sistik
itwiki
Fibrosi cistica
jawiki
嚢胞性線維症
kawiki
კისტური ფიბროზი
kkwiki
Муковисцидоз
kowiki
낭포성 섬유증
liwiki
Tejsliemgekrenkdje
ltwiki
Cistinė fibrozė
lvwiki
Mukoviscidoze
mkwiki
Цистична фиброза
mlwiki
സിസ്റ്റിക് ഫൈബ്രോസിസ്
mswiki
Fibrosis sista
nlwiki
Taaislijmziekte
nnwiki
Cystisk fibrose
nowiki
Cystisk fibrose
orwiki
ସିସ୍ଟିକ୍ ଫାଇବ୍ରୋସିସ୍
plwiki
Mukowiscydoza
ptwiki
Fibrose cística
rowiki
Fibroză chistică
ruwiki
Муковисцидоз
shwiki
Cistična fibroza
simplewiki
Cystic fibrosis
skwiki
Cystická fibróza
slwiki
Cistična fibroza
sqwiki
Fibroza kistike
srwiki
Цистична фиброза
svwiki
Cystisk fibros
swwiki
Uvimbe wa fibrosisi
szywiki
masatawasiay ku lebawa
thwiki
ซิสติก ไฟโบรซิส
tlwiki
Sistikong pibrosis
trwiki
Kistik fibrozis
ukwiki
Муковісцидоз
uzwiki
Mukovitsidoz
viwiki
Xơ nang
zh_yuewiki
囊性纖維化
zhwiki
囊腫性纖維化
Wikibooks
(1 entry)
edit
slwikibooks
Cistična fibroza
Wikinews
(1 entry)
edit
ruwikinews
Категория:Муковисцидоз
Wikiquote
(1 entry)
edit
slwikiquote
Cistična fibroza
Wikisource
(0 entries)
edit
Wikiversity
(0 entries)
edit
Wikivoyage
(0 entries)
edit
Wiktionary
(0 entries)
edit
Multilingual sites
(0 entries)
edit
Retrieved from "
https://www.wikidata.org/w/index.php?title=Q178194&oldid=2412399998
"
Search
Search
cystic fibrosis
(Q178194)
Add topic
[8]
ページ先頭
©2009-2025
Movatter.jp