About: inherited blood coagulation disease

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

Human disease

Attributes	Values
rdf:type	Item
description	Human disease (en) хвороба людини (uk)
exact match	wds:Q18555031-B887E766-2F71-4BFA-B5CE-C1E5F8B7C92F wds:Q18555031-D62BCD50-A9B3-40A6-A51E-EEFFC79D25F7 wds:Q18555031-EFE096EE-65AB-442A-9516-7CB1FF08B63B
exact match	http://www.orpha.net/ORDO/Orphanet_98429
health specialty	wds:Q18555031-57348516-65ED-4E6B-9105-F525157649CE wds:Q18555031-EE4EFB69-2CCA-40C3-ACE3-6B3D2068E812
Mondo ID	wds:Q18555031-76BDC537-3B6A-4F8C-90B6-BD562A80FDE7
Disease Ontology ID	wds:Q18555031-0D899C0C-3FA1-418C-B9CF-128A3A35E5CE
Mondo ID	http://purl.obolibrary.org/obo/MONDO_0021181
health specialty	medical genetics hematology
Mondo ID	MONDO_0021181
rdfs:label	enfermedad hereditaria de la coagulación sanguínea (es) dedna bolezen strjevanja krvi (sl) inherited blood coagulation disease (en) malaltia hereditària de la coagulació sanguínia (ca) troubles héréditaires de la coagulation sanguine (fr) 遺伝性血液凝固疾患 (ja)
skos:prefLabel	enfermedad hereditaria de la coagulación sanguínea (es) dedna bolezen strjevanja krvi (sl) inherited blood coagulation disease (en) malaltia hereditària de la coagulació sanguínia (ca) troubles héréditaires de la coagulation sanguine (fr) 遺伝性血液凝固疾患 (ja)
name	enfermedad hereditaria de la coagulación sanguínea (es) dedna bolezen strjevanja krvi (sl) inherited blood coagulation disease (en) malaltia hereditària de la coagulació sanguínia (ca) troubles héréditaires de la coagulation sanguine (fr) 遺伝性血液凝固疾患 (ja)
instance of	wds:Q18555031-5625FCBA-EFFE-4FB6-ABC5-7A80E38314AE
instance of	class of disease
subclass of	wds:Q18555031-1C265A00-D915-4A32-9083-A7A24C81C65A wds:Q18555031-ECD05736-1CEB-4905-B1C0-FAD39BDE63A1
subclass of	blood coagulation disease genetic disease
Orphanet ID	wds:Q18555031-82ECC07C-A1FE-40F3-9618-BB0361C00ECF
Orphanet ID	98429
skos:altLabel	Coagulation Disorder, Hereditary (en) Coagulation Disorder, Inherited (en) Coagulation Disorders, Hereditary (en) Coagulation Disorders, Inherited (en) Hereditary Blood Coagulation Disorders (en) Hereditary Coagulation Disorder (en) Hereditary Coagulation Disorders (en) Inherited Blood Coagulation Disorders (en) Inherited Coagulation Disorder (en) Inherited Coagulation Disorders (en) congenital bleeding disorder (en) hereditary blood coagulation disease (en) inherited blood coagulation disorder (en) 遺伝性血液凝固異常 (ja)
NCI Thesaurus ID	wds:Q18555031-c49664ae-4c74-9c75-41e4-03a956ab4989
UMLS CUI	wds:Q18555031-10ce4767-4ad1-4712-cb6d-11c27e19faf8 wds:Q18555031-4C93E308-CE4B-4A94-9A55-ADE4FE1A92C9 wds:Q18555031-E6E1FDD2-5AE5-49FD-8706-57B0496D832A
MeSH descriptor ID	wds:Q18555031-E5C2221E-E3B5-409C-A1C1-C9974FF7EC86
on focus list of Wikimedia project	wds:Q18555031-D424ED18-FB2D-4CC4-B312-517FA724DF11
MeSH tree code	wds:Q18555031-0F31CC06-BE72-4BA3-8AE2-DB0B7CE048F7 wds:Q18555031-24302CF5-8E15-4741-80D0-72190AE4F358
MeSH descriptor ID	http://id.nlm.nih.gov/mesh/D025861
MeSH tree code	http://id.nlm.nih.gov/mesh/C15.378.100.100 http://id.nlm.nih.gov/mesh/C16.320.099
NCI Thesaurus ID	C103172
UMLS CUI	C0852077 C5681721
MeSH descriptor ID	D025861
on focus list of Wikimedia project	WikiProject Medicine
MeSH tree code	C15.378.100.100 C16.320.099
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q18555031
is subclass of of	antithrombin III deficiency factor XIII deficiency Factor V Leiden protein C deficiency hemophilia B congenital afibrinogenemia hemophilia von Willebrand's disease factor X deficiency gray platelet syndrome Quebec platelet disorder Bernard-Soulier syndrome Factor I Deficiency Glanzmann's thrombasthenia factor VII deficiency Scott syndrome Owren's disease platelet-type bleeding disorder 3 platelet-type bleeding disorder 10 platelet-type bleeding disorder 18 platelet-type bleeding disorder 15 platelet-type bleeding disorder 19 platelet-type bleeding disorder 16 platelet-type bleeding disorder 8 platelet-type bleeding disorder 14 platelet-type bleeding disorder 17

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