SHMARQL

cystic fibrosis

<http://www.wikidata.org/entity/Q178194>

autosomal recessive disease characterized by the buildup of mucus
cystic fibrosis
rdfs:label
"cystic fibrosis"@en
skos:altLabel
"CF"@en
"CYSTIC FIBROSIS"@en
"CYSTIC FIBROSIS; CF"@en
"mucoviscidosis"@en
schema:description
"autosomal recessive disease characterized by the buildup of mucus"@en
schema:dateModified "2026-11-10T17:06:17+00:00"^^xsd:dateTime
schema:version 2567626599
wikibase:identifiers 85
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wdt:P1617 "53613dfc-58c9-4e1e-9151-182db224111f"
wdt:P1692 "277.0"
wdt:P1748 "C2975"
wdt:P18 <http://commons.wikimedia.org/wiki/Special:FilePath/ClubbingCF.JPG>
wdt:P1995 medical genetics
pediatrics
pulmonology
wdt:P2004 "31334"
wdt:P2176 tobramycin
dornase alfa
N-acetyl-L-cysteine
aztreonam
amiloride
ivacaftor
elexacaftor/ivacaftor/tezacaftor
sodium phenylbutyrate
wdt:P227 "4040669-6"
wdt:P2293 SERPINA1
CFTR
HMOX1
HFE
TGFB1
MIF
AGTR2
CEACAM3
FCGR2A
GCLC
GSTM3
KCNN4
CEACAM6
SLC8A3
SLC9A3
SLC11A1
STX1A
SLC6A14
CLCA4
DCTN4
AHRR
SLC26A9
EDNRA
wdt:P2347 "26696"
wdt:P244 "sh85035204"
wdt:P268 "11956777v"
wdt:P279 autosomal recessive disease
syndrome
lung disease
genetic biliary tract disease
rare genetic respiratory disease
genetic pancreatic disease
rare male fertility disorder with obstructive azoospermia
rare genetic disorder with obstructive azoospermia
wdt:P2841 any age
wdt:P2888 <http://identifiers.org/doid/DOID:1485>
<http://purl.obolibrary.org/obo/DOID_1485>
<http://www.orpha.net/ORDO/Orphanet_586>
wdt:P2892 "C0010674"
"C0392164"
"C1527396"
wdt:P31 type of disease
symptom or sign
designated intractable/rare disease
wdt:P3201 "10011762"
wdt:P3219 "mucoviscidose-fibrose-kystique-du-pancreas"
wdt:P3222 "cystisk-fibros"
wdt:P3417 "Cystic-Fibrosis"
wdt:P3471 "1329"
wdt:P349 "00570677"
wdt:P3569 "levenswetenschappen-en-geneeskunde/cystische-fibrose"
wdt:P373 "Cystic fibrosis"
wdt:P3827 "cystic-fibrosis"
wdt:P3984 "CysticFibrosis"
wdt:P4229 "E84"
"E84.0"
"E84.1"
"E84.8"
"E84.9"
wdt:P4233 "cystic-fibrosis"
wdt:P4317 "6233"
wdt:P4527 "9540"
wdt:P4746 "028445"
wdt:P4802 "102788"
wdt:P4839 "Entity["Disease", "ICDNine277.0"]"
"Entity["Disease", {"ICDNine277.0", "Primary"}]"
wdt:P486 "D003550"
wdt:P492 "219700"
wdt:P494 "E84"
wdt:P5008 WikiProject Medicine
wdt:P5019 "zystische-fibrose"
wdt:P508 "20386"
wdt:P5082 "cystisk_fibrose"
wdt:P5270 "MONDO_0009061"
wdt:P557 "3347"
wdt:P5806 "190905008"
wdt:P604 "000107"
wdt:P6200 "c207p54ml5gt"
wdt:P6366 "2910021119"
"2910515979"
wdt:P646 "/m/0dcp_"
wdt:P6532 cor pulmonale
Infantile onset
dehydration
rectal prolapse
childhood onset
elevated transaminases
obstructive lung disease
abnormal liver storage
wdt:P665 "H00218"
wdt:P667 "T99"
wdt:P668 "NBK1250"
wdt:P672 "C06.689.202"
"C08.381.187"
"C16.320.190"
"C16.614.213"
wdt:P673 "1001602"
wdt:P691 "ph119277"
wdt:P699 "DOID:1485"
wdt:P7033 "scot/16747"
wdt:P7329 "CA25"
wdt:P7464 "cystic-fibrosis"
wdt:P7502 "Cystic_fibrosis-X9MMB"
wdt:P780 cholestasis
pneumonia
hepatitis
liver cirrhosis
bowel obstruction
osteoporosis
peptic ulcer disease
bronchitis
heart failure
dyspnea
cyanosis
muscle weakness
gallstone
pulmonary fibrosis
bronchiectasis
atelectasis
wdt:P7807 "514403112"
wdt:P7982 "11965"
wdt:P7995 "cystic-fibrosis"
wdt:P8189 "987007538476705171"
wdt:P8313 "cystisk_fibrose"
wdt:P8408 "CysticFibrosis"
wdt:P8814 "14178988-n"
wdt:P910 Category:Cystic fibrosis
wdt:P920 "LEM201003805"
wdt:P923 screening
Sweat test
physical examination
wdt:P9322 "h0008225-cysticka-fibroza"
wdt:P950 "XX534572"
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