SHMARQL

X-linked intellectual disability

<http://www.wikidata.org/entity/Q8041560>

syndromic intellectual characterized by an X-linked inheritance pattern
rdfs:label
"X-linked intellectual disability"@en
skos:altLabel
"Mental Retardation, X-Linked"@en
"syndromic X-linked intellectual disability"@en
"syndromic X-linked mental retardation"@en
"syndromic intellectual disability, X-linked"@en
schema:description
"syndromic intellectual characterized by an X-linked inheritance pattern"@en
schema:dateModified "2026-07-05T13:04:02+00:00"^^xsd:dateTime
schema:version 2514129264
wikibase:identifiers 12
wikibase:sitelinks 7
wikibase:statements 32
p:P10376 wd:statement/Q8041560-C04892C2-C087-47EE-9249-BB712E6B7F9E
p:P11143 wd:statement/Q8041560-F9FAF607-ADA1-44B6-A990-6BF9A23E47D8
p:P1550 wd:statement/Q8041560-31B5178D-6324-4439-A7BD-82A6AC993B58
p:P1995 wd:statement/Q8041560-466F4651-D6C1-4CD1-96D0-F409A4351484
wd:statement/Q8041560-4D7E248E-766D-4DD9-98E4-1D2EDC93D6FF
p:P2293 wd:statement/Q8041560-1EF285F9-5469-4CA5-A2FD-8B03B2A252CA
wd:statement/Q8041560-6B5A9065-F6BD-478F-B13C-31BDEDB6D208
wd:statement/Q8041560-6E8B5758-63B1-4F3A-B790-8045F07F52D8
wd:statement/Q8041560-7429FE24-7930-4CC2-A196-1828084D7598
wd:statement/Q8041560-A1267778-AD62-470C-9303-60105C6E21F7
wd:statement/Q8041560-A80A3BA6-3FC8-4012-A9E1-25801B2BEDFC
wd:statement/Q8041560-BE7F9784-26AB-4BE4-A5C2-2426AD5A9EFC
wd:statement/Q8041560-C02EF1BF-0D22-4706-B824-A089D729EAD1
p:P279 wd:statement/Q8041560-044049D1-57F4-4F87-8EC0-78FC72EB01F0
wd:statement/Q8041560-D742A734-D523-4BE9-8F42-73E406D52027
wd:statement/Q8041560-ad99fa85-47af-bea6-9be0-3761e04e1a9d
wd:statement/Q8041560-b6955adc-4d40-271a-3f7a-829de9c0a335
p:P2888 wd:statement/Q8041560-8743E3A3-89E5-4778-B23E-1FEC03F4AF37
wd:statement/Q8041560-8EA1C171-E199-46FC-A03E-AEC0ACB60AF2
wd:statement/Q8041560-96390D5C-2268-4F3D-991D-70A22BB84A76
p:P2892 wd:statement/Q8041560-7CA4EA23-90FA-4C7D-953D-B047A66589F5
p:P31 wd:statement/Q8041560-2AEF2FE9-0270-40B7-81AE-1007BDA2BCB9
wd:statement/Q8041560-B57F2EBA-FF7A-4A4F-97E1-5BF390C9052B
p:P486 wd:statement/Q8041560-6fece945-47e0-e7a4-7e44-c33648cb1f89
p:P5008 wd:statement/Q8041560-6C3E0424-96C7-4359-BED5-AD39E431435E
p:P5270 wd:statement/Q8041560-04844A99-4C60-4418-AB6E-0B7A6F9C75F0
p:P6366 wd:statement/Q8041560-89892702-9DA4-4E37-B57A-68F37AB12538
p:P665 wd:statement/Q8041560-35E013E3-34EC-4765-A7DF-7FFE190E8189
p:P672 wd:statement/Q8041560-7F6CC07B-5896-443C-9CF8-037AE1753751
wd:statement/Q8041560-DB6FCE5F-63BB-45F7-A7D2-10E09FEECF01
wd:statement/Q8041560-E8C0FDAB-5350-4A5F-91E4-2ABBD29DB4BD
p:P699 wd:statement/Q8041560-4B919363-B888-4AF6-BC1C-B91D81F247C4
p:direct-normalized/P486 <http://id.nlm.nih.gov/mesh/D038901>
p:direct-normalized/P5270 <http://purl.obolibrary.org/obo/MONDO_0020119>
p:direct-normalized/P6366 <https://makg.org/entity/2779277417>
p:direct-normalized/P665 <http://www.kegg.jp/entry/H00658>
p:direct-normalized/P672 <http://id.nlm.nih.gov/mesh/C10.597.606.360.455>
<http://id.nlm.nih.gov/mesh/C16.320.322.500>
<http://id.nlm.nih.gov/mesh/C16.320.400.525>
p:direct-normalized/P699 <http://purl.obolibrary.org/obo/DOID_DOID:0060309>
wdt:P10376 "medicine-and-dentistry/x-linked-intellectual-disability"
wdt:P11143 "X-linked intellectual disability"
wdt:P1550 "98464"
wdt:P1995 medical genetics
neurology
wdt:P2293 ARX
DDX3X
PAK3
KDM5C
CASK
AP1S2
ZC4H2
BRWD3
wdt:P279 X-linked disease
genetic syndromic intellectual disability
wdt:P2888 <http://identifiers.org/doid/DOID:0060309>
<http://purl.obolibrary.org/obo/DOID_0060309>
<http://www.orpha.net/ORDO/Orphanet_98464>
wdt:P2892 "C1136249"
wdt:P31 type of disease
rare disease
wdt:P486 "D038901"
wdt:P5008 WikiProject Medicine
wdt:P5270 "MONDO_0020119"
wdt:P6366 "2779277417"
wdt:P665 "H00658"
wdt:P672 "C10.597.606.360.455"
"C16.320.322.500"
"C16.320.400.525"
wdt:P699 "DOID:0060309"
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data from SPARQL profile: Wikidata