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rdfs:label
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"AEC sendromu"@tr
"AEC綜合徵"@zh
"Hay-Wells-Syndrom"@de
"Síndrome de anquiloblefaro-defeitos ectodérmicos-fenda lábio-palatina"@pt
"Síndrome de anquiloblefaro-defeitos ectodérmicos-fenda lábio-palatina"@pt-br
"Zespół Haya-Wellsa"@pl
"ankyloblepharon-ectodermal defects-cleft lip/palate syndrome"@en
"syndrome de Hay-Wells"@fr
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skos:altLabel
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"AEC syndrome"@en
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"Hay-Wells syndrome"@en
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"ankyloblepharon-ectodermal defects-cleft lip and palate syndrome"@en
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schema:description
|
"Krankheit"@de
"human disease"@en
"malattia"@it
"rzadki zespół wad wrodzonych"@pl
"хвороба людини"@uk
"մարդու հիվանդություն"@hy
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schema:dateModified
|
"2026-10-23T23:19:56+00:00"^^xsd:dateTime
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schema:version
|
2560152794
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wikibase:identifiers
|
14
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16
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wikibase:sitelinks
|
4
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wikibase:statements
|
35
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p:P11143
|
wd:statement/Q940210-05910C2B-0F98-4409-A39D-425C13BEEC7D
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|
p:P11430
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wd:statement/Q940210-e3a8a7cb-4ef2-e8cc-8f2b-0c9f2f2f3568
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p:P14914
|
wd:statement/Q940210-D990A2A4-990D-459D-9553-0C12ED9CEC9C
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p:P1550
|
wd:statement/Q940210-bee9fad3-48dc-2e10-07cf-cef0930ca2c2
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p:P1748
|
wd:statement/Q940210-7d42756d-44a8-408c-9a18-4d762647af7e
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p:P1995
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wd:statement/Q940210-8DDB4CE3-02DB-42D9-8AD7-DFABE7E89C0C
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p:P2293
|
wd:statement/Q940210-27A322BF-DA18-4421-AD52-C4A03F84A189
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|
p:P279
|
wd:statement/Q940210-5b61d45e-4c92-b97c-18e0-8d1359f47ef7
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|
wd:statement/Q940210-6A8F6B86-4108-4188-9E98-4F33913381DC
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|
wd:statement/Q940210-d9da447d-4bc8-081a-c207-d22cadd63d35
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|
p:P2841
|
wd:statement/Q940210-1BF0D7F3-4B0A-4BAE-91FA-C86D4D2B08A8
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p:P2888
|
wd:statement/Q940210-5E061251-90DB-42B1-824F-920C5B7F33AF
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|
wd:statement/Q940210-94D05950-5EB9-4371-B6A3-6C1CE97DB8A8
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|
wd:statement/Q940210-DA01C4D1-EFC4-435E-951E-CA1E5D4F07F6
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p:P2892
|
wd:statement/Q940210-BBC00DDE-E88D-4D9A-83C0-43442E6FF642
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p:P31
|
wd:statement/Q940210-3AC974D4-862E-4AEB-A9DB-AB9B569C300B
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|
wd:statement/Q940210-78E486F2-DDA9-4044-9DB4-E636C1AAC1B5
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|
p:P4317
|
wd:statement/Q940210-4A889C39-0C14-4B58-9A66-BB844B6C716E
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|
p:P486
|
wd:statement/Q940210-EDEB8027-51ED-4720-A5E2-F2AC04840166
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|
p:P492
|
wd:statement/q940210-67F666E4-936A-49BE-A783-E2D0C4074A6B
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|
p:P5008
|
wd:statement/Q940210-E0547BCF-1994-4268-BBC2-976E7FB36088
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|
p:P5270
|
wd:statement/Q940210-8232A75D-0478-4893-A15C-E7517BE0F08A
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|
p:P557
|
wd:statement/q940210-04340866-D38F-4A79-B17D-0A41BC390436
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|
p:P6366
|
wd:statement/Q940210-BB62EF0C-65B2-4765-A0CF-835160DD6592
|
|
p:P6532
|
wd:statement/Q940210-0E3569C0-4D58-4DF7-ACBD-A8A5B3CC0840
|
|
wd:statement/Q940210-1331AF87-7C35-4D65-9560-9F4B405493B5
|
|
wd:statement/Q940210-1C8C3CD6-8272-4131-957B-ABA6276D206F
|
|
wd:statement/Q940210-1F18C6EA-0E79-4547-8888-FA198D2EE353
|
|
wd:statement/Q940210-55EC6C18-9CC8-4BF6-A93F-C7F0DC486132
|
|
wd:statement/Q940210-5AC8CFC0-D98D-43C3-A921-7F0345280FFC
|
|
wd:statement/Q940210-9ED33A58-777B-4528-9692-6B3CED9579EE
|
|
p:P665
|
wd:statement/Q940210-7D79274C-DC68-4845-A4F7-48C8429E9F7B
|
|
p:P699
|
wd:statement/Q940210-E2B439A9-F2A0-4B75-B4C1-8F78661A40DF
|
|
p:P7464
|
wd:statement/Q940210-9F6912B3-2134-4754-8456-75DC1EA6A315
|
|
p:P7807
|
wd:statement/Q940210-CDD06157-DCE2-4141-A05A-9313C981729D
|
|
p:direct-normalized/P486
|
<http://id.nlm.nih.gov/mesh/C535289>
|
|
p:direct-normalized/P5270
|
<http://purl.obolibrary.org/obo/MONDO_0007124>
|
|
p:direct-normalized/P6366
|
<https://makg.org/entity/2776338505>
|
|
p:direct-normalized/P665
|
<http://www.kegg.jp/entry/H00752>
|
|
p:direct-normalized/P699
|
<http://purl.obolibrary.org/obo/DOID_DOID:0090119>
|
|
wdt:P11143
|
"Hay–Wells syndrome"
|
|
wdt:P11430
|
"DI-00122"
|
|
wdt:P14914
|
"D01071"
|
|
wdt:P1550
|
"1071"
|
|
wdt:P1748
|
"C157576"
|
|
wdt:P1995
|
medical genetics
|
|
wdt:P2293
|
TP63
|
|
wdt:P279
|
ectodermal dysplasia
|
|
autosomal dominant disease
|
|
syndromic ankyloblepharon
|
|
wdt:P2841
|
neonatal onset
|
|
wdt:P2888
|
<http://identifiers.org/doid/DOID:0090119>
|
|
<http://purl.obolibrary.org/obo/DOID_0090119>
|
|
<http://www.orpha.net/ORDO/Orphanet_1071>
|
|
wdt:P2892
|
"C1785148"
|
|
wdt:P31
|
type of disease
|
|
rare disease
|
|
wdt:P4317
|
"6571"
|
|
wdt:P486
|
"C535289"
|
|
wdt:P492
|
"106260"
|
|
wdt:P5008
|
WikiProject Medicine
|
|
wdt:P5270
|
"MONDO_0007124"
|
|
wdt:P557
|
"33336"
|
|
wdt:P6366
|
"2776338505"
|
|
wdt:P6532
|
Widely spaced teeth
|
|
Finger syndactyly
|
|
Submucous cleft soft palate
|
|
hypohidrosis
|
|
congenital onset
|
|
choanal atresia, bilateral
|
|
familial congenital nasolacrimal duct obstruction
|
|
wdt:P665
|
"H00752"
|
|
wdt:P699
|
"DOID:0090119"
|
|
wdt:P7464
|
"ankyloblepharon-ectodermal-defects-cleft-lip-palate-syndrome"
|
|
wdt:P7807
|
"1008188767"
|