About: factor X deficiency

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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	Krankheit (de) Human disease (en) хвороба людини (uk) مرض يصيب الإنسان (ar)
exact match	wds:Q18555036-1B136B6F-C3DC-4321-B6E4-D0752025FB93 wds:Q18555036-71998EFB-DDF3-4C78-B3B9-EB2FB1FF5FAB wds:Q18555036-9221B1F0-C1FF-4ABD-8AF5-C7673E9EB5CA
exact match	http://purl.obolibrary.org/obo/DOID_2222 http://purl.obolibrary.org/obo/HP_0008321 http://identifiers.org/doid/DOID:2222
health specialty	wds:Q18555036-A5EDCD98-2791-424A-A2B0-DA9D09848AC5 wds:Q18555036-DD4CC263-A3AA-4907-B74E-B5E9C77C9949
Mondo ID	wds:Q18555036-8A7499FD-4331-4B7D-9232-404F02CFFA01
Disease Ontology ID	wds:Q18555036-7AFED6B7-E73B-40A5-A42F-5714CC698AFD
Mondo ID	http://purl.obolibrary.org/obo/MONDO_0002247
Disease Ontology ID	http://purl.obolibrary.org/obo/DOID_DOID:2222
health specialty	medical genetics hematology
Mondo ID	MONDO_0002247
Disease Ontology ID	DOID:2222
rdfs:label	Deficiencia de factor X (es) déficit en facteur X (fr) factor X deficiency (en)
skos:prefLabel	Deficiencia de factor X (es) déficit en facteur X (fr) factor X deficiency (en)
name	Deficiencia de factor X (es) déficit en facteur X (fr) factor X deficiency (en)
instance of	wds:Q18555036-35F81011-D202-421B-82DF-B1F24EABE77D
instance of	class of disease
subclass of	wds:Q18555036-14289413-97F6-4C6B-9BA5-C3E1A70B605C wds:Q18555036-9F8E9BDA-180B-41C7-873E-25B1B0B3BDFF wds:Q18555036-DE39CE15-DD9A-4EE0-B732-EC7BB6094E73
subclass of	blood coagulation disease autosomal recessive disease inherited blood coagulation disease
KEGG ID	wds:Q18555036-8912C6D6-53C7-407D-99E9-49BCFAF764A9
KEGG ID	http://www.kegg.jp/entry/H02257
KEGG ID	H02257
UniProt disease ID	wds:Q18555036-0f73ac15-4a6b-b708-497f-7220aec77afe
Orphanet ID	wds:Q18555036-2645BAE4-7454-43E3-B240-10352CD7EFE9
PatientsLikeMe condition ID	wds:Q18555036-db90f2c5-4ba2-cab8-c573-5ae67be9b67c
GARD rare disease ID	wds:Q18555036-285BA224-4DEC-458B-8D67-2C0B8C0962C5
OMIM ID	wds:Q18555036-F1C9CC93-6D1B-4684-A597-76F65850C879
Genetics Home Reference Conditions ID	wds:Q18555036-BCE0EDED-CF1C-4332-B2F4-C1F0B5F08D0F
UniProt disease ID	DI-03028
Orphanet ID	328
PatientsLikeMe condition ID	factor-x-deficiency
GARD rare disease ID	6404
OMIM ID	227600
Genetics Home Reference Conditions ID	factor-x-deficiency
Human Phenotype Ontology ID	wds:Q18555036-66D55403-2869-42EB-9683-8545711C8680
Human Phenotype Ontology ID	HP:0008321
skos:altLabel	Factor X deficiency (en) Deficiencia del factor Stuart-Prower (es) Factor X deficiency (disorder) (en) disease, Stuart-Prower (en)
NCI Thesaurus ID	wds:Q18555036-3ED4F606-A1D0-4A24-B05E-17B444A107DE wds:Q18555036-40FDB17B-7B6E-4739-B585-A16FA7422B91 wds:Q18555036-66f0794c-44df-acef-161f-e1e32170df94
UMLS CUI	wds:Q18555036-24D3C531-A035-44FA-99A4-0BA92536B4A0 wds:Q18555036-A01808A3-2208-48F7-910B-AEAB9CF32E05
MeSH descriptor ID	wds:Q18555036-D55C11DB-8302-4889-AF11-AA37F94C718D
on focus list of Wikimedia project	wds:Q18555036-01720396-F4D0-4C7B-95BA-63F5C181F542
MedlinePlus ID	wds:Q18555036-4694A100-8586-437A-AF1B-2004B927CEC5
Microsoft Academic ID	wds:Q18555036-2393B911-C109-4873-8EAE-4BB9AA3ED335
MeSH tree code	wds:Q18555036-7F072DD7-16F6-4AB6-A7C9-8EEC24F8C0BC wds:Q18555036-8374B9E0-9685-4899-8DC9-199C081EC925 wds:Q18555036-9FFF56EA-B182-4A11-AF3D-91D5F4879AFB wds:Q18555036-E015438B-82CC-40FD-A069-305AA52950B0
DeCS ID	wds:Q18555036-77679D51-9632-4F15-8A14-C4FA3B2D66B4
MeSH descriptor ID	http://id.nlm.nih.gov/mesh/D005171
Microsoft Academic ID	https://makg.org/entity/2777577732
MeSH tree code	http://id.nlm.nih.gov/mesh/C15.378.100.100.320 http://id.nlm.nih.gov/mesh/C15.378.100.141.320 http://id.nlm.nih.gov/mesh/C15.378.463.320 http://id.nlm.nih.gov/mesh/C16.320.099.320
NCI Thesaurus ID	C131632 C98940
UMLS CUI	C0015519 C4024702
MeSH descriptor ID	D005171
on focus list of Wikimedia project	WikiProject Medicine
MedlinePlus ID	000553
Microsoft Academic ID	2777577732
MeSH tree code	C15.378.100.100.320 C15.378.100.141.320 C15.378.463.320 C16.320.099.320
DeCS ID	5271
WikiProjectMed ID	wds:Q18555036-E82DF57C-7655-43A9-B87F-25B743DACFA3
WikiProjectMed ID	Factor X deficiency
is owl:sameAs of	factor X deficiency
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q18555036 Factor X deficiency https://es.wikipedia.org/wiki/Deficiencia_de_factor_X
is subclass of of	acquired factor X deficiency
is subclass of of	wds:Q55789510-d6c28525-4ae7-9dfb-6adf-602430093dd3

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