About: lipoprotein glomerulopathy

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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) մարդու հիվանդություն (hy) хвороба людини (uk)
exact match	wds:Q11699959-C4E7D7A1-6E67-4008-AB99-F8E022CF742F
exact match	http://www.orpha.net/ORDO/Orphanet_329481
Mondo ID	wds:Q11699959-FAF6230C-E8CF-4D98-8881-005EB85D42BE
Mondo ID	http://purl.obolibrary.org/obo/MONDO_0012725
Mondo ID	MONDO_0012725
rdfs:label	Glomerulopatia lipoproteinowa (pl) glomérulopathie lipoprotéinique (fr) lipoprotein glomerulopathy (en) 脂蛋白肾病 (zh) 脂蛋白肾病 (zh-cn)
skos:prefLabel	Glomerulopatia lipoproteinowa (pl) glomérulopathie lipoprotéinique (fr) lipoprotein glomerulopathy (en) 脂蛋白肾病 (zh) 脂蛋白肾病 (zh-cn)
name	Glomerulopatia lipoproteinowa (pl) glomérulopathie lipoprotéinique (fr) lipoprotein glomerulopathy (en) 脂蛋白肾病 (zh) 脂蛋白肾病 (zh-cn)
instance of	wds:Q11699959-238720CF-48FB-4D09-AAA4-3C845142116A wds:Q11699959-BD9EBD95-4A0A-4D52-81E3-E588EF907425
instance of	class of disease rare disease
subclass of	wds:Q11699959-54BD6179-C7B8-49D4-A991-591C5C8E9D7A wds:Q11699959-755b945b-403c-8cbb-d561-662a5f1fc409 wds:Q11699959-C680741A-6F08-40CD-842B-75C6EB74DC52
subclass of	lipid metabolism disorder syndromic dyslipidemia primary glomerular disease
KEGG ID	wds:Q11699959-A6AD5D32-BD79-4EAB-96D2-A17F49852CED
KEGG ID	http://www.kegg.jp/entry/H00887
KEGG ID	H00887
UniProt disease ID	wds:Q11699959-ab5eee7b-4947-729b-6c31-58e86de8738a
Orphanet ID	wds:Q11699959-ddf177e4-4c7d-61f7-e463-e616a0822c90
ICD-9-CM	wds:Q11699959-569F0AE6-7B16-480E-85CF-4173299D6395 wds:Q11699959-A8014266-C4DC-4F6E-B1D5-E3DEC9B53D61
genetic association	wds:Q11699959-DBE0F3A6-BEEA-4E4D-8DA7-B514F712B99A
ICD-10-CM	wds:Q11699959-4791E965-7F8F-419A-9294-9DF78654A07E
OMIM ID	wds:Q11699959-a2231c38-42c0-9979-29c9-d9b7c09d2c48
UniProt disease ID	DI-01910
Orphanet ID	329481
ICD-9-CM	593.89 272.8
genetic association	APOE
ICD-10-CM	N07.8
OMIM ID	611771
skos:altLabel	LPG (en) Glomérulopathie à lipoprotéines (fr) LIPOPROTEIN GLOMERULOPATHY (en) LIPOPROTEIN GLOMERULOPATHY; LPG (en)
Encyclopedia of China (Third Edition) ID	wds:Q11699959-EE0A347D-BC9D-46E8-AE79-C53C79081605
UMLS CUI	wds:Q11699959-C2F8067F-11C8-4BC4-924B-8C2363D8B82E
MeSH descriptor ID	wds:Q11699959-CB73727D-EA33-4D3A-B924-2A6F5D7127A7
ICD-11 ID (MMS)	wds:Q11699959-DD3CF3BF-3694-4C16-8C7C-7A372D521F41
ICD-11 (foundation)	wds:Q11699959-40691303-5E1B-453F-875D-5EB2E9F433F3
MeSH descriptor ID	http://id.nlm.nih.gov/mesh/C567089
Encyclopedia of China (Third Edition) ID	213077
UMLS CUI	C2673196
MeSH descriptor ID	C567089
ICD-11 ID (MMS)	MF82
ICD-11 (foundation)	69778702
is about of	https://pl.wikipedia.org/wiki/Glomerulopatia_lipoproteinowa https://www.wikidata.org/wiki/Special:EntityData/Q11699959
is main subject of	Lipoprotein glomerulopathy: a new apolipoprotein E mutation with enhanced glomerular binding Apolipoprotein E Sendai (arginine 145-->proline): a new variant associated with lipoprotein glomerulopathy Association of a novel 3-amino acid deletion mutation of apolipoprotein E (Apo E Tokyo) with lipoprotein glomerulopathy Lipoprotein glomerulopathy treated with LDL-apheresis (Heparin-induced Extracorporeal Lipoprotein Precipitation system): a case report Lipoprotein glomerulopathy: first case in a white European APOE Kyoto mutation in European Americans with lipoprotein glomerulopathy Successful treatment of patients with lipoprotein glomerulopathy by protein A immunoadsorption: a pilot study Lipoprotein glomerulopathy associated with a mutation in apolipoprotein e Apolipoprotein E mutations: a comparison between lipoprotein glomerulopathy and type III hyperlipoproteinemia Diminished LDL receptor and high heparin binding of apolipoprotein E2 Sendai associated with lipoprotein glomerulopathy Impact of lipoprotein glomerulopathy on the relationship between lipids and renal diseases Clinical and pathological analyses of lipoprotein glomerulopathy Lipoprotein glomerulopathy: glomerular lipoprotein thrombi in a patient with hyperlipoproteinemia Hereditary features, treatment, and prognosis of the lipoprotein glomerulopathy in patients with the APOE Kyoto mutation. Virus-mediated transduction of apolipoprotein E (ApoE)-sendai develops lipoprotein glomerulopathy in ApoE-deficient mice Lipoprotein glomerulopathy induced by ApoE-Sendai is different from glomerular lesions in aged apoE-deficient mice Chronic graft-versus-host autoimmune disease in Fc receptor gamma chain-deficient mice results in lipoprotein glomerulopathy Apolipoprotein E2/E5 variants in lipoprotein glomerulopathy recurred in transplanted kidney Abnormal lipoprotein and apolipoprotein pattern in lipoprotein glomerulopathy Thermodynamic and structural destabilization of apoE3 by hereditary mutations associated with the development of lipoprotein glomerulopathy Topics in lipoprotein glomerulopathy: an overview A Case of Lipoprotein Glomerulopathy with apoE Chicago and apoE (Glu3Lys) Treated with Fenofibrate A case of lipoprotein glomerulopathy with a rare apolipoprotein E isoform combined with neurofibromatosis type I. Macrophage impairment produced by Fc receptor gamma deficiency plays a principal role in the development of lipoprotein glomerulopathy in concert with apoE abnormalities A new apolipoprotein E mutation, apoE Las Vegas, in a European-American with lipoprotein glomerulopathy A novel apolipoprotein E mutation (p.Arg150Cys) in a Chinese patient with lipoprotein glomerulopathy A novel variant apolipoprotein E Okayama in a patient with lipoprotein glomerulopathy A novel apolipoprotein E mutation, ApoE Tsukuba (Arg 114 Cys), in lipoprotein glomerulopathy Atherosclerosis, inflammation and lipoprotein glomerulopathy in kidneys of apoE-/-/LDL-/- double knockout mice [Clinicopathologic study of 8 cases of lipoprotein glomerulopathy] A new variant of apolipoprotein E (apo E Maebashi) in lipoprotein glomerulopathy Common apolipoprotein E gene mutations contribute to lipoprotein glomerulopathy in China

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