About: Scott syndrome

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

inherited blood coagulation disease

Attributes	Values
rdf:type	Item
owl:sameAs	Scott syndrome
description	inherited blood coagulation disease (en) choroba genetyczna (pl)
exact match	wds:Q7437571-A872F0FC-49D4-466A-82C3-094FB7BDF7C6 wds:Q7437571-ADFF3B60-B71D-4621-8CA0-45671B50918A wds:Q7437571-E732ED4E-8551-43E3-BF1E-721438CFE289
exact match	http://purl.obolibrary.org/obo/DOID_0111052 http://identifiers.org/doid/DOID:0111052 http://www.orpha.net/ORDO/Orphanet_806
Mondo ID	wds:Q7437571-C3DAFF7B-979E-442B-ABF7-B2D41F08FB53
DiseasesDB	wds:Q7437571-59F0F995-EC34-490B-896E-ABE5416F16C1
Disease Ontology ID	wds:Q7437571-2FA182B2-388F-4C5C-9F99-D00251A67CEC
Mondo ID	http://purl.obolibrary.org/obo/MONDO_0009885
Disease Ontology ID	http://purl.obolibrary.org/obo/DOID_DOID:0111052
Mondo ID	MONDO_0009885
DiseasesDB	32153
Disease Ontology ID	DOID:0111052
rdfs:label	Scott syndrome (en) Scott-Syndrom (de) sindromo de Scott (eo) syndrome de Scott (fr) zespół Scotta (pl) متلازمة سكوت (ar)
skos:prefLabel	Scott syndrome (en) Scott-Syndrom (de) sindromo de Scott (eo) syndrome de Scott (fr) zespół Scotta (pl) متلازمة سكوت (ar)
name	Scott syndrome (en) Scott-Syndrom (de) sindromo de Scott (eo) syndrome de Scott (fr) zespół Scotta (pl) متلازمة سكوت (ar)
instance of	wds:Q7437571-C1D99CE5-BF0D-4708-9C26-60A299B8FEFA wds:Q7437571-D481BD2A-CEBB-4A51-81F2-2E3D100CFB36
instance of	class of disease rare disease
subclass of	wds:Q7437571-AA505C1A-B0B5-4181-9D2B-189CC6981214 wds:Q7437571-F3D7924B-0279-4584-90D1-4DE8943B3F71 wds:Q7437571-f18e857d-469d-da0d-ffa1-0a7d42e9ce5f
subclass of	blood coagulation disease inherited blood coagulation disease rare hemorrhagic disorder due to a qualitative platelet defect
KEGG ID	wds:Q7437571-12846BF5-5928-4CCE-A01F-D581C6390492
KEGG ID	http://www.kegg.jp/entry/H01162
KEGG ID	H01162
UniProt disease ID	wds:Q7437571-e00957e2-4374-87f2-ca90-2710d69ec5ee
Orphanet ID	wds:Q7437571-965266E9-6F7D-401D-A9B2-2FBEF14EAFE5
genetic association	wds:Q7437571-FD56439F-79FA-4581-BEBE-55F724A54BD2
ICD-10-CM	wds:Q7437571-A1BBCE9A-2250-45A1-AD67-404EA7FC7DDC
GARD rare disease ID	wds:Q7437571-D0A3E6B7-F091-45D9-AE82-2876973F3CB5
OMIM ID	wds:Q7437571-3B39EEAA-04E2-42B0-98C3-9FBDFAECB27B
UniProt disease ID	DI-03017
Orphanet ID	806
genetic association	ANO6
ICD-10-CM	D69.8
GARD rare disease ID	4777
OMIM ID	262890
skos:altLabel	BDPLT7 (en) SCTS (en) bleeding abnormality due to deficiency of platelet biding of factor X (en) Bleeding Disorder, Platelet-Type, 7 (en) Platelet factor X receptor deficiency (en) Prothrombin Consumption Inhibitor, Familial (en) Prothrombin Conversion Defect, Familial (en) SCOTT SYNDROME (en) SCOTT SYNDROME; SCTS (en) familial prothrombin consumption inhibitor (en) familial prothrombin conversion defect (en) platelet-type bleeding disorder 7 (en) prothrombin consumption deficiency (en) Bleeding Abnormality Due to Deficiency of Platelet Binding of Factor 10 (en)
UMLS CUI	wds:Q7437571-A9CD6EF5-E1F5-40A5-8FBD-B192A1676C74
MeSH descriptor ID	wds:Q7437571-A956A9EA-CB6A-40FA-8AF6-0F69FB757AA8 wds:Q7437571-EBC93E68-5D93-4EF3-BAEF-784E7CBBF032
on focus list of Wikimedia project	wds:Q7437571-55C74453-76E2-4D7C-92A1-5144E722AE36
Microsoft Academic ID	wds:Q7437571-2249238D-D9FE-474E-A5E6-3EE5FA2948C5
ICD-11 (foundation)	wds:Q7437571-b387b2af-4e65-88b4-c2f6-c8c9d10e06ae
MeSH descriptor ID	http://id.nlm.nih.gov/mesh/C563120
Microsoft Academic ID	https://makg.org/entity/2779651361
UMLS CUI	C0796149
MeSH descriptor ID	C563120
on focus list of Wikimedia project	WikiProject Medicine
Microsoft Academic ID	2779651361
ICD-11 (foundation)	186013982
is owl:sameAs of	Scott syndrome
is about of	Scott syndrome https://pl.wikipedia.org/wiki/Zesp%C3%B3%C5%82_Scotta https://www.wikidata.org/wiki/Special:EntityData/Q7437571 Scott syndrome https://de.wikipedia.org/wiki/Scott-Syndrom https://ar.wikipedia.org/wiki/%D9%85%D8%AA%D9%84%D8%A7%D8%B2%D9%85%D8%A9_%D8%B3%D9%83%D9%88%D8%AA
is main subject of	A genome-wide linkage scan in German shepherd dogs localizes canine platelet procoagulant deficiency (Scott syndrome) to canine chromosome 27. Scott syndrome, a bleeding disorder caused by defective scrambling of membrane phospholipids Assembly of the platelet prothrombinase complex is linked to vesiculation of the platelet plasma membrane. Studies in Scott syndrome: an isolated defect in platelet procoagulant activity Defective Ca(2+)-induced microvesiculation and deficient expression of procoagulant activity in erythrocytes from a patient with a bleeding disorder: a study of the red blood cells of Scott syndrome Scott syndrome: a disorder of platelet coagulant activity.

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