SHMARQL

primary ciliary dyskinesia

<http://www.wikidata.org/entity/Q1690779>

ciliopathy with impaired function of the cilia lining the respiratory tract and fallopian tube
rdfs:label
"primary ciliary dyskinesia"@en
skos:altLabel
"PCD"@en
"ciliary motility disorder"@en
"ciliary motility disorders"@en
"immotile ciliary syndrome"@en
schema:description
"ciliopathy with impaired function of the cilia lining the respiratory tract and fallopian tube"@en
schema:dateModified "2026-10-23T23:45:08+00:00"^^xsd:dateTime
schema:version 2560157957
wikibase:identifiers 25
27
wikibase:sitelinks 12
wikibase:statements 95
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wd:statement/Q1690779-B7D3CB1A-53DB-4F99-8769-D45BD7400CDC
wd:statement/Q1690779-CB3F7287-A418-4010-8539-55B859FB120F
wd:statement/Q1690779-CB80CB3E-AE56-45CF-B7BA-0DD236200D08
wd:statement/Q1690779-CB82BA89-C2EA-4246-AB25-43670B18E6C2
wd:statement/Q1690779-CD6DF54D-B626-483A-AEC0-0792FFD53012
wd:statement/Q1690779-D1869973-1D20-49AD-B781-31BCC4C28EA7
wd:statement/Q1690779-D1951C08-E065-422C-AC2F-9E637E10F134
wd:statement/Q1690779-D3C1A0D5-0008-4697-82EB-4AFD201ADE16
wd:statement/Q1690779-D892779D-C116-45D9-8779-DF2AB799EACE
wd:statement/Q1690779-DD03E3B4-C2FD-40A5-87CB-AE2F4B64F80B
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wd:statement/Q1690779-FE6B328A-AAA8-4027-9921-C04150A86199
p:P279 wd:statement/Q1690779-6ECC4281-8C44-4A34-8624-7F5C49232A7E
p:P2841 wd:statement/Q1690779-9C48D38F-98C6-44E0-A3FA-1225BBF9048D
p:P2888 wd:statement/Q1690779-1A04277A-17DC-410A-A965-201D9D28F212
wd:statement/Q1690779-1A9FCD74-5823-4BC7-9CC2-2D893A6A4117
wd:statement/Q1690779-C5860D0D-CB8F-4F52-9574-6BC9373E213E
wd:statement/Q1690779-E6BBADAB-3E29-4867-B6F7-D321B29F86C0
p:P2892 wd:statement/Q1690779-A973325E-DBDE-4A6E-9608-DF563F36D8C4
p:P31 wd:statement/Q1690779-1B6B95BC-C002-4A47-B12F-74D07557B51D
p:P3201 wd:statement/Q1690779-1CF96CCF-D394-4FF8-A7B0-5F2BA91C1393
p:P373 wd:statement/Q1690779-342a8d91-4455-ab32-62f5-ea343370f2a9
p:P3827 wd:statement/Q1690779-9A146F9B-8919-409E-8F3B-ABCA94CDC49F
p:P3841 wd:statement/Q1690779-BED2D12A-7CC7-4B6A-88E4-C6B5366D1AB1
p:P4317 wd:statement/Q1690779-80F949AC-E468-4460-9EF8-F8A8CA98D2FE
p:P486 wd:statement/Q1690779-8F378023-4D3D-4C5D-89EA-77E663E006AD
p:P493 wd:statement/q1690779-B0DB7419-2590-4740-B8BC-07014122A979
p:P494 wd:statement/q1690779-F60A14DA-0C34-4354-8F93-C1550958772B
p:P5008 wd:statement/Q1690779-BB7F1F65-D59C-4F90-9CF8-D911EFCF385E
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wd:statement/q1690779-9A882E47-B1F5-40C9-A380-038840F7DD5F
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p:P6532 wd:statement/Q1690779-2FD479E4-248E-49E8-80FB-FCC2AC68CEDC
p:P665 wd:statement/Q1690779-B5B729B4-5C37-4F72-84A3-ECA97DA4DA2A
p:P672 wd:statement/Q1690779-44720D9F-675C-49D9-9FCF-B4CBB49E9318
wd:statement/Q1690779-980740FC-CC85-4F33-A7E6-9F49EFDC2875
wd:statement/Q1690779-D8C5FA85-94B0-4458-9CD1-0F154D89C1DE
wd:statement/Q1690779-F35EF474-80FD-4E4F-A5DE-C086EFE4061B
p:P673 wd:statement/q1690779-F1EEABF4-BF29-4EA0-9A95-F55899BCDC8D
p:P699 wd:statement/Q1690779-809F6306-773E-42D6-910E-91D19118BA97
p:P7329 wd:statement/Q1690779-c7d812fc-42a6-453b-b89c-0e5adda7b15d
p:P7464 wd:statement/Q1690779-1AF60B8D-08F3-493C-8FFE-417BCC0225BC
p:P7807 wd:statement/Q1690779-8846A5E8-F745-4D4A-8129-F5DD2183E9F6
p:direct-normalized/P3201 <http://purl.bioontology.org/ontology/MDRFRE/10040761>
p:direct-normalized/P486 <http://id.nlm.nih.gov/mesh/D002925>
p:direct-normalized/P665 <http://www.kegg.jp/entry/H00564>
p:direct-normalized/P672 <http://id.nlm.nih.gov/mesh/C08.200>
<http://id.nlm.nih.gov/mesh/C09.150>
<http://id.nlm.nih.gov/mesh/C16.131.077.245.500>
<http://id.nlm.nih.gov/mesh/C16.320.184.500>
p:direct-normalized/P699 <http://purl.obolibrary.org/obo/DOID_DOID:9562>
wdt:P10283 "C2778206077"
"C2908520674"
wdt:P11143 "Primary ciliary dyskinesia"
wdt:P1193 0.0003^^xsd:decimal
wdt:P14914 "D00244"
wdt:P1550 "244"
wdt:P1748 "C84638"
wdt:P1995 pulmonology
wdt:P2293 SPEF2
TP73
CENPF
DNAH5
DNAH9
FOXJ1
GAS8
RPGR
SPAG1
NME5
OFD1
DNAH11
CCNO
DNAAF11
DNAH1
DNAI1
STK36
NME8
ZMYND10
BRWD1
HYDIN
DNAAF5
TTC12
CCDC40
ARMC4
DNAAF2
DNAH7
CFAP298
DNAI2
CLXN
ODAD4
DNAL1
RSPH3
CFAP300
CFAP74
CCDC65
RSPH1
DRC1
ODAD1
LRRC56
ODAD3
DNAAF1
DNAAF6
CFAP54
NEK10
DNAAF4
DAW1
CFAP221
RSPH9
GAS2L2
CCDC39
MCIDAS
RSPH4A
DNAAF3
DNAJB13
CCDC103
wdt:P279 ciliopathy
wdt:P2841 neonatal onset
wdt:P2888 <http://identifiers.org/doid/DOID:9562>
<http://purl.obolibrary.org/obo/DOID_9562>
<http://purl.obolibrary.org/obo/HP_0012265>
<http://www.orpha.net/ORDO/Orphanet_244>
wdt:P2892 "C0008780"
wdt:P31 type of disease
wdt:P3201 "10040761"
wdt:P373 "Primary ciliary dyskinesia"
wdt:P3827 "ciliary-motility-disorders"
wdt:P3841 "HP:0012265"
wdt:P4317 "4484"
wdt:P486 "D002925"
wdt:P493 "759.3"
wdt:P494 "Q89.3"
wdt:P5008 WikiProject Medicine
wdt:P557 "29887"
"7111"
wdt:P646 "/m/02zpv7"
wdt:P6532 respiratory tract infection
wdt:P665 "H00564"
wdt:P672 "C08.200"
"C09.150"
"C16.131.077.245.500"
"C16.320.184.500"
wdt:P673 "1002319"
wdt:P699 "DOID:9562"
wdt:P7329 "CB40.0"
wdt:P7464 "primary-ciliary-dyskinesia"
wdt:P7807 "955573234"
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