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rdfs:label
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"CD3gamma deficiency"@en
"Imunodeficiência combinada por deficiência em CD3 gama"@pt
"Imunodeficiência combinada por deficiência em CD3 gama"@pt-br
"déficit immunitaire combiné par déficit en CD3gamma"@fr
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skos:altLabel
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"CD3 deficiency"@en
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|
"Cd3-Gamma Deficiency"@en
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"IMD17"@en
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"IMMUNODEFICIENCY 17"@en
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|
"IMMUNODEFICIENCY 17; IMD17"@en
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|
"Immunodeficiency type 17"@en
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|
"SCID-Like Immunodeficiency, T Cell-Partial, B Cell-Positive, Nk Cell-Positive"@en
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|
"immunodeficiency 17"@en
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schema:description
|
"Human disease"@en
"Krankheit"@de
"хвороба людини"@uk
"մարդու հիվանդություն"@hy
"مرض يصيب الإنسان"@ar
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schema:dateModified
|
"2026-10-23T23:29:53+00:00"^^xsd:dateTime
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schema:version
|
2560155300
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wikibase:identifiers
|
11
|
|
wikibase:sitelinks
|
0
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wikibase:statements
|
32
|
|
p:P11430
|
wd:statement/Q18553596-99cd99e8-4de8-84a6-4986-39f413092daa
|
|
p:P14914
|
wd:statement/Q18553596-95083D94-C203-4125-B57D-904112947168
|
|
p:P1550
|
wd:statement/Q18553596-6658bfd0-411d-9304-b7ed-b5e11f2f13bc
|
|
p:P2293
|
wd:statement/Q18553596-74ADB960-9091-43E2-839A-8161C578CFB0
|
|
p:P279
|
wd:statement/Q18553596-14FB5155-3614-4EEE-AB83-B1B6C1A7415D
|
|
wd:statement/Q18553596-6E7A8602-035B-4DE7-8859-FAEC32E50B9F
|
|
wd:statement/Q18553596-C4504879-14C1-4F0B-A2E7-B8C270172AC4
|
|
wd:statement/Q18553596-D966A4A3-8960-432F-B3C0-A1ED83F5FAAD
|
|
p:P2841
|
wd:statement/Q18553596-19EDE3FF-4414-488E-93DD-FC4A7FD608EE
|
|
p:P2888
|
wd:statement/Q18553596-0D4BF2B4-461C-4DDC-8818-0410C82CED01
|
|
wd:statement/Q18553596-2F5DF948-591D-4A3A-85A7-8BA7AD77A704
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|
wd:statement/Q18553596-414DC1E5-3E4D-4D74-A5B8-08005B95E076
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|
wd:statement/Q18553596-9C6001B5-A385-4174-BA93-529665AED819
|
|
wd:statement/Q18553596-F263BA12-8BCB-4093-BE35-1E430D218C0C
|
|
p:P2892
|
wd:statement/Q18553596-5043FBD2-1DD2-4830-8F3B-A22800208AF8
|
|
wd:statement/Q18553596-D26C18BF-2855-471F-BB76-8C5019C3E287
|
|
p:P31
|
wd:statement/Q18553596-C7D00728-AD89-421F-AA47-859B8E01FC20
|
|
wd:statement/Q18553596-DB24C990-6229-41A9-9018-E2C139CD18EC
|
|
p:P4229
|
wd:statement/Q18553596-09E5FE39-9649-4533-AA11-A59FC66E45E7
|
|
p:P4317
|
wd:statement/Q18553596-46334781-4B24-4432-8C9E-B03C103F390C
|
|
p:P492
|
wd:statement/Q18553596-C758E844-DEA2-4CC0-B52A-89E0C6930BC2
|
|
p:P5008
|
wd:statement/Q18553596-D94C7B65-0201-42A1-AEEF-F30EAC939493
|
|
p:P5270
|
wd:statement/Q18553596-982DBAD8-B672-4916-84BB-F28A5FE02BF8
|
|
p:P6532
|
wd:statement/Q18553596-145A4B78-210D-49AD-99A8-979EBA357376
|
|
wd:statement/Q18553596-1719164B-49AE-4BCB-8B4E-307F9F0B5B4B
|
|
wd:statement/Q18553596-2C295661-20DF-446A-936B-DD2BDD613D36
|
|
wd:statement/Q18553596-61D88BEC-EC09-4C88-99F9-D072DAA678E4
|
|
wd:statement/Q18553596-6334BB31-24AC-49D8-A94D-F4F476B376CB
|
|
wd:statement/Q18553596-F09BB846-670A-468F-BDB7-83FB41426CA0
|
|
wd:statement/Q18553596-F2015184-1078-4CA5-AEAF-7D4D017DEE03
|
|
p:P699
|
wd:statement/Q18553596-1FB69820-38BF-46D1-B5F4-C147B74B06D0
|
|
wd:statement/Q18553596-43FF94A6-7527-43F9-85AE-E4E841B3D0C9
|
|
p:direct-normalized/P5270
|
<http://purl.obolibrary.org/obo/MONDO_0014276>
|
|
p:direct-normalized/P699
|
<http://purl.obolibrary.org/obo/DOID_DOID:0060018>
|
|
<http://purl.obolibrary.org/obo/DOID_DOID:0111973>
|
|
wdt:P11430
|
"DI-04033"
|
|
wdt:P14914
|
"D169082"
|
|
wdt:P1550
|
"169082"
|
|
wdt:P2293
|
CD3G
|
|
wdt:P279
|
autosomal recessive disease
|
|
severe combined immunodeficiency
|
|
non-severe combined immunodeficiency
|
|
T cell deficiency
|
|
wdt:P2841
|
infantile onset
|
|
wdt:P2888
|
<http://identifiers.org/doid/DOID:0060018>
|
|
<http://identifiers.org/doid/DOID:0111973>
|
|
<http://purl.obolibrary.org/obo/DOID_0060018>
|
|
<http://purl.obolibrary.org/obo/DOID_0111973>
|
|
<http://www.orpha.net/ORDO/Orphanet_169082>
|
|
wdt:P2892
|
"C2025557"
|
|
"C3810107"
|
|
wdt:P31
|
type of disease
|
|
rare disease
|
|
wdt:P4229
|
"D81.2"
|
|
wdt:P4317
|
"9521"
|
|
wdt:P492
|
"615607"
|
|
wdt:P5008
|
WikiProject Medicine
|
|
wdt:P5270
|
"MONDO_0014276"
|
|
wdt:P6532
|
chronic diarrhea
|
|
Recurrent otitis media
|
|
Recurrent respiratory infections
|
|
Recurrent oral thrush
|
|
failure to thrive
|
|
autoimmune hemolytic anemia
|
|
intestinal disease
|
|
wdt:P699
|
"DOID:0060018"
|
|
"DOID:0111973"
|