|
rdfs:label
|
"Sindrome di Strømme"@it
"Stromme sendromu"@tr
"Stromme syndrome"@en
"Strømme-Syndrom"@de
"Strømmov sindrom"@sl
"Síndrome de malformação fetal cerebral fatal – atresia duodenal – hipoplasia renal bilateral"@pt
"Síndrome de malformação fetal cerebral fatal – atresia duodenal – hipoplasia renal bilateral"@pt-br
"syndrome de malformation cérébrale-atrésie duodénale-hypoplasie rénale bilatérale fœtal létal"@fr
"Ստրոմմեի համախտանիշ"@hy
"متلازمة ستروم"@ar
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|
skos:altLabel
|
"CILD31"@en
|
|
"Stromme Syndrome"@en
|
|
"apple peel syndrome with microcephaly and ocular anomalies"@en
|
|
"jejunal atresia with microcephaly and ocular anomalies"@en
|
|
"lethal fetal brain malformation-duodenal atresia-bilateral renal hypoplasia syndrome"@en
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|
"primary ciliary dyskinesia 31"@en
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schema:description
|
"human disease"@en
"menschliche Krankheit"@de
"хвороба людини"@uk
"مرض يصيب الإنسان"@ar
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|
schema:dateModified
|
"2026-10-24T00:19:42+00:00"^^xsd:dateTime
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|
schema:version
|
2560164806
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|
wikibase:identifiers
|
12
|
|
wikibase:sitelinks
|
7
|
|
wikibase:statements
|
26
|
|
p:P11430
|
wd:statement/Q28024726-0ab399c9-41fa-d480-91fc-a3410c9eda1b
|
|
p:P1193
|
wd:statement/Q28024726-20204218-1603-4B7C-BA77-5BCCE447A549
|
|
p:P11956
|
wd:statement/Q28024726-EB96FBBC-E4F6-47C9-8DF0-A0B6DD5C4BE2
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|
p:P14914
|
wd:statement/Q28024726-33E7E3CE-2401-4F48-8759-7ABB3DEE09CF
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|
p:P1550
|
wd:statement/Q28024726-6f0c501d-4cb5-1958-cd4e-463922b325f1
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|
p:P1995
|
wd:statement/Q28024726-6FD2E0D7-AAE3-47F7-9714-45D6FAFB8B2E
|
|
p:P2293
|
wd:statement/Q28024726-5733500E-0345-4AC8-A933-B10EF93E9FB4
|
|
p:P279
|
wd:statement/Q28024726-1ec82de7-4d72-1fce-04f4-86ea1d12a359
|
|
wd:statement/Q28024726-C4882749-3158-4C57-AD3E-50FA0ABE78BA
|
|
p:P2841
|
wd:statement/Q28024726-C2DE09B0-0F80-402E-BA35-3C9E3D399A0E
|
|
p:P2888
|
wd:statement/Q28024726-942774DA-225D-4888-8714-29F44E8AC56F
|
|
wd:statement/Q28024726-C870019B-CF1D-4DF7-BF04-2DF3BB2CD4FB
|
|
p:P2892
|
wd:statement/Q28024726-5DC9D211-CBA5-48FF-9980-5CA267921B6D
|
|
wd:statement/Q28024726-B8020677-5C17-4CA3-BB7E-4B0DA16FC989
|
|
p:P31
|
wd:statement/Q28024726-05A6618E-B8ED-40EF-9BEB-151D8D8B67E5
|
|
wd:statement/Q28024726-5B78593F-20ED-4D80-94EE-E6E3B1B7A73F
|
|
p:P373
|
wd:statement/Q28024726-0946fb8c-e8d2-4b59-862f-5ea1c19c8156
|
|
p:P4229
|
wd:statement/Q28024726-E8437493-A55B-4400-9B60-64618E1B6F40
|
|
p:P486
|
wd:statement/Q28024726-93808DA6-1941-4B0D-825E-CEBC8932ADFB
|
|
p:P492
|
wd:statement/Q28024726-8CF10FBD-356C-48CC-84D2-8D091EBCDFDD
|
|
p:P5008
|
wd:statement/Q28024726-0C6080AD-7EEA-4B19-A2D5-7033D0DCCDBA
|
|
p:P5270
|
wd:statement/Q28024726-15965EE9-7E7F-410D-B25A-429F0D7AF78D
|
|
p:P6532
|
wd:statement/Q28024726-53E86F57-41A2-4BF2-AE56-A946CBFD81D0
|
|
wd:statement/Q28024726-85AC746C-9E68-4934-80D7-37ADB098A84E
|
|
p:P665
|
wd:statement/Q28024726-DB208C5B-07FB-45B3-AC38-83C7A4F2E697
|
|
p:P699
|
wd:statement/Q28024726-6B4BA3BA-76E6-4EA3-89AF-28CAC54D763F
|
|
p:direct-normalized/P486
|
<http://id.nlm.nih.gov/mesh/C565460>
|
|
p:direct-normalized/P5270
|
<http://purl.obolibrary.org/obo/MONDO_0009477>
|
|
p:direct-normalized/P665
|
<http://www.kegg.jp/entry/H01814>
|
|
p:direct-normalized/P699
|
<http://purl.obolibrary.org/obo/DOID_DOID:0110595>
|
|
wdt:P11430
|
"DI-04686"
|
|
wdt:P1193
|
0.000001^^xsd:decimal
|
|
wdt:P11956
|
"0009160"
|
|
wdt:P14914
|
"D444069"
|
|
wdt:P1550
|
"444069"
|
|
wdt:P1995
|
medical genetics
|
|
wdt:P2293
|
CENPF
|
|
wdt:P279
|
duodenal atresia
|
|
primary ciliary dyskinesia
|
|
wdt:P2841
|
congenital onset
|
|
wdt:P2888
|
<http://identifiers.org/doid/DOID:0110595>
|
|
<http://purl.obolibrary.org/obo/DOID_0110595>
|
|
wdt:P2892
|
"C1855705"
|
|
"C5681197"
|
|
wdt:P31
|
type of disease
|
|
rare disease
|
|
wdt:P373
|
"Strømme syndrome"
|
|
wdt:P4229
|
"Q87.8"
|
|
wdt:P486
|
"C565460"
|
|
wdt:P492
|
"243605"
|
|
wdt:P5008
|
WikiProject Medicine
|
|
wdt:P5270
|
"MONDO_0009477"
|
|
wdt:P6532
|
accessory spleen
|
|
Preaxial polydactyly
|
|
wdt:P665
|
"H01814"
|
|
wdt:P699
|
"DOID:0110595"
|