SHMARQL

syndrome with combined immunodeficiency

<http://www.wikidata.org/entity/Q55787698>

human disease
rdfs:label
"syndrome with combined immunodeficiency"@en
schema:description
"human disease"@en
schema:dateModified "2026-10-24T00:08:38+00:00"^^xsd:dateTime
schema:version 2560162864
wikibase:identifiers 4
wikibase:sitelinks 0
wikibase:statements 7
p:P14914 wd:statement/Q55787698-A09FFDEF-D851-4108-B3C0-DCCC174144CE
p:P1550 wd:statement/Q55787698-D0EE318C-CCC3-48ED-921A-038EAF84832E
p:P279 wd:statement/Q55787698-8F37921D-E5A0-400C-AAD1-61B16BDFDBA7
p:P2888 wd:statement/Q55787698-8C87A1ED-26EF-48A5-B809-C9C7F58C1B80
p:P2892 wd:statement/Q55787698-31C78C8E-CB0B-435D-8B04-2FE2701F9326
p:P31 wd:statement/Q55787698-63ECB228-9875-45EF-BABA-677F1BC3F146
p:P5270 wd:statement/Q55787698-D64C51E9-FAAA-4725-A0B7-5521974ED489
p:direct-normalized/P5270 <http://purl.obolibrary.org/obo/MONDO_0018035>
wdt:P14914 "D331217"
wdt:P1550 "331217"
wdt:P279 primary immunodeficiency due to a defect in adaptive immunity
wdt:P2888 <http://www.orpha.net/ORDO/Orphanet_331217>
wdt:P2892 "C2711630"
wdt:P31 type of disease
wdt:P5270 "MONDO_0018035"
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