SHMARQL

facial cleft

<http://www.wikidata.org/entity/Q5428558>

congenital abnormality consisting of an opening or gap in the face, which results from incomplete fusion of one or more of the embryonic facial prominences
rdfs:label
"facial cleft"@en
skos:altLabel "CLEFT FACE"@en
"Craniofacial cleft"@en
"Prosoposchisis"@en
schema:description
"congenital abnormality consisting of an opening or gap in the face, which results from incomplete fusion of one or more of the embryonic facial prominences"@en
schema:dateModified "2026-10-23T23:24:50+00:00"^^xsd:dateTime
schema:version 2560154240
wikibase:identifiers 10
15
wikibase:sitelinks 5
wikibase:statements 28
p:P10565 wd:statement/Q5428558-2768d975-486f-8d61-6fcd-d43ab01404f0
p:P1368 wd:statement/Q5428558-c8f655a4-4d5c-a4ea-1c85-128a0ca83242
p:P14541 wd:statement/Q5428558-A418137C-7032-4BA0-8804-656A95DA1BC7
p:P14914 wd:statement/Q5428558-36069880-3A90-4792-9A69-2C349FF95B94
p:P1550 wd:statement/Q5428558-e6b1470d-4883-4485-57fa-bc7e2d9ca7a2
p:P1748 wd:statement/Q5428558-2CAFFBF8-963F-47A9-9951-0147CE04418A
p:P2293 wd:statement/Q5428558-21C3DB97-E389-44C9-8FEA-AFDD6EDD2AF5
wd:statement/Q5428558-9EC5DE75-06C4-4E33-BB63-AE8857A0D4A7
wd:statement/Q5428558-D1E53AD4-987F-4F6A-A449-C82983CE26AF
p:P279 wd:statement/Q5428558-11d0dad3-4d25-eeb6-d932-ce94e733e2dc
wd:statement/Q5428558-2375C4A4-832B-4483-A6D4-168671B7F6CB
wd:statement/Q5428558-54ca2a25-43db-2219-7a12-b869fbe36a53
wd:statement/Q5428558-D0B24E42-5F6E-42DC-9BF7-5206D5267CD3
wd:statement/Q5428558-DEB96DAB-74C2-4F4C-B870-F64ABB2BE0EF
wd:statement/Q5428558-F268BF77-6B70-4524-9D13-503555683378
p:P2888 wd:statement/Q5428558-F0C4B710-4B6A-4CA3-A491-41E9F5FB4D9E
p:P2892 wd:statement/Q5428558-C42ED619-9CAE-487C-B883-E8C666CB60CF
p:P31 wd:statement/Q5428558-E299073C-ED21-41B3-86C8-DF0F518AE210
p:P373 wd:statement/Q5428558-a5246e93-43f3-a9b2-5dd6-05628250b506
p:P3841 wd:statement/Q5428558-95DF8D7D-137F-4DF9-B4C7-D48428A61601
p:P4229 wd:statement/Q5428558-741099A1-8769-497B-86F1-A6BBE49D792D
p:P5008 wd:statement/Q5428558-336589E9-2613-4287-B23E-130EBEDC35AC
p:P5270 wd:statement/Q5428558-27C0CEFB-AA43-4B64-8DA8-A7B58CB7E032
p:P6366 wd:statement/Q5428558-C867B2F7-EC13-4889-8E53-8625BB5EF025
p:P691 wd:statement/Q5428558-101C6C0A-FAF2-4E6D-A1D1-F19942FD29CB
p:P7329 wd:statement/Q5428558-D08F6720-A257-4311-9CEF-BE6578CDE24E
p:P7807 wd:statement/Q5428558-EE9CF50E-7BE4-435B-BC61-2F0ABCF0DE2E
p:P9322 wd:statement/Q5428558-BA496B53-63C6-47FE-8E6D-7B4402CE6C92
p:direct-normalized/P5270 <http://purl.obolibrary.org/obo/MONDO_0015411>
p:direct-normalized/P6366 <https://makg.org/entity/2779246384>
wdt:P10565 "601554"
wdt:P1368 "000351110"
wdt:P14541 "2kLMbT"
wdt:P14914 "D141229"
wdt:P1550 "141229"
wdt:P1748 "C124510"
wdt:P2293 PTCH2
SPECC1L
FREM1
wdt:P279 facial feature
rare head and neck malformation
rare maxillo-facial surgical disease
developmental failure of fusion
wdt:P2888 <http://www.orpha.net/ORDO/Orphanet_141229>
wdt:P2892 "C0685787"
wdt:P31 type of disease
wdt:P373 "Facial cleft"
wdt:P3841 "HP:0002006"
wdt:P4229 "Q18.8"
wdt:P5008 concrete/abstract disjunction anomalies
wdt:P5270 "MONDO_0015411"
wdt:P6366 "2779246384"
wdt:P691 "ph125281"
wdt:P7329 "LA51"
wdt:P7807 "11389088"
wdt:P9322 "h0004055-rozstep-obliceje"
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data from SPARQL profile: Wikidata