SHMARQL

Glanzmann's thrombasthenia

<http://www.wikidata.org/entity/Q1529258>

human disease
rdfs:label
"Glanzmann's thrombasthenia"@en
skos:altLabel
"BDPLT2"@en
"Bleeding Disorder, Platelet-Type, 2"@en
"GLANZMANN THROMBASTHENIA; GT"@en
"GT"@en
"Glanzmann thrombasthenia"@en
"Glycoprotein Complex Iib-Iiia, Deficiency of"@en
"Glycoprotein IIb/IIIa defect"@en
"Gp Iib-Iiia Complex, Deficiency of"@en
"Platelet Fibrinogen Receptor, Deficiency of"@en
"Thrombasthenia"@en
"Thrombocytasthenia"@en
"deficiency of GP IIb-IIIa complex"@en
"deficiency of glycoprotein complex IIb-IIIa"@en
"deficiency of platelet fibrinogen receptor"@en
"platelet glycoprotein IIb-IIIa deficiency"@en
"platelet-type bleeding disorder 2"@en
"thrombasthenia of Glanzmann and Naegeli"@en
schema:description
"human disease"@en
schema:dateModified "2026-10-24T00:38:16+00:00"^^xsd:dateTime
schema:version 2560167554
wikibase:identifiers 33
35
wikibase:sitelinks 14
wikibase:statements 59
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wd:statement/Q1529258-B612A910-0E30-43B0-B70A-9CCD0979F9BB
p:P2888 wd:statement/Q1529258-32CB452B-992A-4BEE-9C16-289B5BE91B81
wd:statement/Q1529258-36968CD3-6A31-4DE6-8A66-B8B4BBF3A4B0
wd:statement/Q1529258-4CA9E7E7-F110-49A0-BE15-89B6A2E1683E
wd:statement/Q1529258-546FB26F-3BE5-4311-8978-55ED5D6FFFBA
wd:statement/Q1529258-A437B58F-3CC4-4C7E-B0F4-7382B1C7BDFC
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wd:statement/Q1529258-55DF9167-1F78-47A5-BD7E-239004781A36
wd:statement/Q1529258-B6E12D22-4ADD-42E1-8933-6071E7CA3C82
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p:P3841 wd:statement/Q1529258-3A682EB1-DC21-4FAE-98CA-FEA0B285B4AB
wd:statement/Q1529258-D011423F-E3EC-42F2-8360-33B54E3A2030
p:P4229 wd:statement/Q1529258-86FF17D6-C1C4-4636-BB6A-33D96B38CDE2
p:P4233 wd:statement/Q1529258-038dfa94-4620-424c-97f5-9e73bdad08a8
p:P4317 wd:statement/Q1529258-FB677361-303C-4099-A0A9-958B4127A2FC
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p:P492 wd:statement/Q1529258-6BAAA16B-721A-412D-A16E-520ADB41DDB7
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p:P557 wd:statement/q1529258-72FF81C5-EF8A-4A6C-BF28-EEF8DE50D77B
p:P604 wd:statement/q1529258-FCADD98A-8493-4D0A-BEC0-9686642D0053
p:P61 wd:statement/Q1529258-25e01c24-4805-8cb6-7cc0-f9fa36197810
p:P6366 wd:statement/Q1529258-B88929BB-FD6C-4B51-B829-346A8D8CE7A5
p:P646 wd:statement/Q1529258-230E301B-40E5-4643-B3A9-D735ED3CFC52
p:P6532 wd:statement/Q1529258-5AB37667-E0B9-4F2E-9653-E21D741D5230
wd:statement/Q1529258-6BB23D1D-6508-4C1E-954C-37DD04AD9448
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wd:statement/Q1529258-E8480018-61A1-428E-8627-BE767B65A811
p:P665 wd:statement/Q1529258-FF54FBBE-EF2A-41D8-946E-2592B605F6BC
p:P672 wd:statement/Q1529258-87746A11-609B-46E5-9E12-EC41808D4C69
wd:statement/Q1529258-90E7BF7A-454A-43C1-8177-CF6E43C0A611
wd:statement/Q1529258-C103D0A1-B540-4ABB-AE69-F5D89ABF8DD5
wd:statement/Q1529258-DD8F3B5F-342E-4A7E-8A79-E6B3FBEF73AB
p:P673 wd:statement/q1529258-FF460426-3679-4F46-ADAB-B86CE9E8C7EC
p:P699 wd:statement/Q1529258-F331FC43-AEA4-49A6-BE0A-CFA45BE92D16
p:P7464 wd:statement/Q1529258-E7663B3C-E514-408D-9B6A-B7A2286ABD4E
p:P8814 wd:statement/Q1529258-fccff87d-4748-83ee-1167-154df415ccd3
p:direct-normalized/P2581 <http://babelnet.org/rdf/s00077075n>
p:direct-normalized/P486 <http://id.nlm.nih.gov/mesh/D013915>
p:direct-normalized/P5270 <http://purl.obolibrary.org/obo/MONDO_0010119>
p:direct-normalized/P6366 <https://makg.org/entity/2778198917>
p:direct-normalized/P665 <http://www.kegg.jp/entry/H00226>
p:direct-normalized/P672 <http://id.nlm.nih.gov/mesh/C15.378.100.100.820>
<http://id.nlm.nih.gov/mesh/C15.378.140.810>
<http://id.nlm.nih.gov/mesh/C15.378.463.810>
<http://id.nlm.nih.gov/mesh/C16.320.099.820>
p:direct-normalized/P699 <http://purl.obolibrary.org/obo/DOID_DOID:2219>
p:direct-normalized/P8814 <http://wordnet-rdf.princeton.edu/rdf/id/14193199-n>
wdt:P10283 "C2778198917"
"C2911156200"
wdt:P11143 "Glanzmann's thrombasthenia"
wdt:P138 Eduard Glanzmann
wdt:P1417 "science/Glanzmanns-thrombasthenia"
wdt:P14914 "D00849"
wdt:P1550 "849"
wdt:P1583 "glanzmann_thrombasthenia"
wdt:P1748 "C61249"
wdt:P1995 hematology
wdt:P2293 ITGB3
ITGA2B
wdt:P2581 "00077075n"
wdt:P279 inherited blood coagulation disease
rare hemorrhagic disorder due to a qualitative platelet defect
wdt:P2841 neonatal onset
infantile onset
wdt:P2888 <http://identifiers.org/doid/DOID:2219>
<http://purl.obolibrary.org/obo/DOID_2219>
<http://purl.obolibrary.org/obo/HP_0001872>
<http://purl.obolibrary.org/obo/HP_0001975>
<http://www.orpha.net/ORDO/Orphanet_849>
wdt:P2892 "C0040015"
"C0151854"
"C4020863"
"C4021767"
wdt:P31 type of disease
wdt:P3841 "HP:0001872"
"HP:0001975"
wdt:P4229 "D69.1"
wdt:P4233 "glanzmann-s-thrombasthenia"
wdt:P4317 "2478"
wdt:P486 "D013915"
wdt:P492 "273800"
wdt:P493 "287.1"
wdt:P5008 WikiProject Medicine
wdt:P5270 "MONDO_0010119"
wdt:P557 "5224"
wdt:P604 "001305"
wdt:P61 Eduard Glanzmann
wdt:P6366 "2778198917"
wdt:P646 "/m/03g3mf"
wdt:P6532 ecchymosis
Spontaneous, recurrent epistaxis
bleeding gums
menorrhagia
gastrointestinal bleeding
macrohematuria
purpura
wdt:P665 "H00226"
wdt:P672 "C15.378.100.100.820"
"C15.378.140.810"
"C15.378.463.810"
"C16.320.099.820"
wdt:P673 "200311"
wdt:P699 "DOID:2219"
wdt:P7464 "glanzmann-thrombasthenia"
wdt:P8814 "14193199-n"
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