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rdfs:label
|
"Atresia-multiplex-congenita-Syndrom"@de
"atrésies gastro-intestinales multiples"@fr
"multiple intestinal atresia"@en
|
|
skos:altLabel
|
"CID-MIA/early-onset IBD"@en
|
|
"Combined immunodeficiency-enteropathy spectrum"@en
|
|
"Familial intestinal polyatresia syndrome"@en
|
|
"Familial multiple intestinal atresia"@en
|
|
"GASTROINTESTINAL DEFECTS AND IMMUNODEFICIENCY SYNDROME"@en
|
|
"GASTROINTESTINAL DEFECTS AND IMMUNODEFICIENCY SYNDROME; GIDID"@en
|
|
"GIDID"@en
|
|
"Intestinal Atresia, Multiple"@en
|
|
"Intestinal Atresia, Multiple And/Or Inflammatory Bowel Disease With or Without Immunodeficiency"@en
|
|
"Intestinal atresia multiple"@en
|
|
"Multiple gastrointestinal atresias"@en
|
|
"Multiple gastrointestinal atresias (disorder)"@en
|
|
schema:description
|
"Human disease"@en
"Krankheit"@de
"хвороба людини"@uk
"مرض يصيب الإنسان"@ar
|
|
schema:dateModified
|
"2026-07-05T12:46:57+00:00"^^xsd:dateTime
|
|
schema:version
|
2514125052
|
|
wikibase:identifiers
|
14
|
|
wikibase:sitelinks
|
2
|
|
wikibase:statements
|
29
|
|
p:P1550
|
wd:statement/Q18554801-7E5652F8-185E-442F-B1C6-899C8CAD7175
|
|
wd:statement/Q18554801-ef96fa23-40dc-c9f6-1f12-6299b381f6ef
|
|
p:P1692
|
wd:statement/Q18554801-E705A465-1C5F-4041-AA03-1AA8E5AC0D3D
|
|
p:P2293
|
wd:statement/Q18554801-4DC2315E-5094-45C1-9287-1C276FFC401E
|
|
p:P279
|
wd:statement/Q18554801-51E4A464-481D-4668-9ABE-AFCEA26DD43D
|
|
wd:statement/Q18554801-64D46155-1371-454B-893C-738832781747
|
|
wd:statement/Q18554801-75C5F5C0-6A49-42C6-8AAF-629183FD2E9C
|
|
wd:statement/Q18554801-BAB5326A-D4BF-476C-ACFE-A0C2906206AE
|
|
wd:statement/Q18554801-C51C4A62-F7EA-485B-B289-22DE4F164D0E
|
|
p:P2888
|
wd:statement/Q18554801-05D2F521-A952-4276-8584-A24C743DA562
|
|
wd:statement/Q18554801-4D64A9E2-3C9A-4B16-A4B2-D738B7E57837
|
|
wd:statement/Q18554801-D1DCD98F-50C6-44F3-B19E-B132D290AC78
|
|
wd:statement/Q18554801-DFDCBC0F-023F-4FC1-8BC1-E15355746866
|
|
p:P2892
|
wd:statement/Q18554801-E4D3C119-38FF-429C-91D4-9F1E2BED6689
|
|
wd:statement/Q18554801-EC1542F8-D4EC-4F50-835C-443DCC4E2C09
|
|
p:P31
|
wd:statement/Q18554801-35D526DA-0222-45D1-B9ED-ECC1F5D9E699
|
|
wd:statement/Q18554801-E2060357-43BC-47AD-ABA4-61E739059EC0
|
|
p:P4229
|
wd:statement/Q18554801-42D93BE7-7EF8-4275-86B3-CE356D88EDD4
|
|
wd:statement/Q18554801-577E232F-BD1D-414D-86D6-CE28FFFC72F8
|
|
p:P4317
|
wd:statement/Q18554801-5565BC0C-CB40-4FDC-838B-62EEAC03B4FC
|
|
p:P486
|
wd:statement/Q18554801-AEBA82F8-8ABC-4CA0-917E-D12794BE58A8
|
|
p:P492
|
wd:statement/Q18554801-932AC99F-4749-4E67-AE75-7221035B91EE
|
|
p:P5008
|
wd:statement/Q18554801-5B446827-59E9-4C39-9C6A-4FD34F6B7699
|
|
p:P5270
|
wd:statement/Q18554801-29310772-26E7-411A-90DB-D1C9F5F6B12B
|
|
p:P6366
|
wd:statement/Q18554801-F3FB707A-AC92-486A-8EF3-B81790847386
|
|
p:P646
|
wd:statement/Q18554801-ECB4DD56-C2C6-4249-A9BA-992B4A5A0029
|
|
p:P665
|
wd:statement/Q18554801-F3750B0F-1194-4FA1-B2B8-7890E3EA6B2C
|
|
p:P699
|
wd:statement/Q18554801-C3AA6D5C-778E-47A3-B30D-DAAC83A9B3D4
|
|
p:P780
|
wd:statement/Q18554801-0c31794f-4aaa-fe84-51fb-54308dc04920
|
|
p:direct-normalized/P486
|
<http://id.nlm.nih.gov/mesh/C562441>
|
|
p:direct-normalized/P5270
|
<http://purl.obolibrary.org/obo/MONDO_0009465>
|
|
p:direct-normalized/P6366
|
<https://makg.org/entity/2910976413>
|
|
p:direct-normalized/P665
|
<http://www.kegg.jp/entry/H02331>
|
|
p:direct-normalized/P699
|
<http://purl.obolibrary.org/obo/DOID_DOID:14671>
|
|
wdt:P1550
|
"2300"
|
|
"436252"
|
|
wdt:P1692
|
"751.8"
|
|
wdt:P2293
|
TTC7A
|
|
wdt:P279
|
autosomal recessive disease
|
|
non-syndromic intestinal malformation
|
|
syndrome with combined immunodeficiency
|
|
wdt:P2888
|
<http://identifiers.org/doid/DOID:14671>
|
|
<http://purl.obolibrary.org/obo/DOID_14671>
|
|
<http://www.orpha.net/ORDO/Orphanet_2300>
|
|
<http://www.orpha.net/ORDO/Orphanet_436252>
|
|
wdt:P2892
|
"C0220744"
|
|
"C5680044"
|
|
wdt:P31
|
type of disease
|
|
rare disease
|
|
wdt:P4229
|
"Q43.8"
|
|
"Q82.8"
|
|
wdt:P4317
|
"3013"
|
|
wdt:P486
|
"C562441"
|
|
wdt:P492
|
"243150"
|
|
wdt:P5008
|
WikiProject Medicine
|
|
wdt:P5270
|
"MONDO_0009465"
|
|
wdt:P6366
|
"2910976413"
|
|
wdt:P646
|
"/m/012kcn0h"
|
|
wdt:P665
|
"H02331"
|
|
wdt:P699
|
"DOID:14671"
|
|
wdt:P780
|
intestinal atresia
|