About: rare dyslipidemia

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

Rare lipid metabolism disorder

Attributes	Values
rdf:type	Item
description	Rare lipid metabolism disorder (en)
exact match	wds:Q55785266-5BC0757B-16CA-4BB8-AD0A-D0AF1BA7DA4A
exact match	http://www.orpha.net/ORDO/Orphanet_101953
drug or therapy used for treatment	wds:Q55785266-5DD63E6F-DC94-42F0-9B86-628CFF382644 wds:Q55785266-72DBCADB-D778-4CCB-BF21-61F1F0C7C603 wds:Q55785266-74D7D569-E8B8-466E-B78E-EAB00ECAEA28 wds:Q55785266-765DC884-387A-40C3-9645-CF879FCFCBD2 wds:Q55785266-7C2F786A-387D-440E-92D9-7BA751E21CE1 wds:Q55785266-89F95083-EBEF-4C39-88DE-C2A39F5A1DC4 wds:Q55785266-98A851AB-033F-4DAA-B21D-6B89E4D54E54 wds:Q55785266-A1E16379-B540-4CD0-BD97-963E622D9755 wds:Q55785266-CF0F0841-4323-4DDB-BDE8-DFEAF6791C78
Mondo ID	wds:Q55785266-92878940-A3FF-4758-BC71-B672C82F9B8B
Mondo ID	http://purl.obolibrary.org/obo/MONDO_0015123
drug or therapy used for treatment	rosuvastatin evolocumab fenofibrate wd:Q668093 pravastatin ezetimibe pitavastatin amlodipine / atorvastatin ezetimibe / simvastatin
Mondo ID	MONDO_0015123
rdfs:label	dislipidemia rara (es) dislipèmia rara (ca) rare dyslipidemia (en) redka dislipidemija (sl) اعتلال ليبيدات الدم النادر (ar)
skos:prefLabel	dislipidemia rara (es) dislipèmia rara (ca) rare dyslipidemia (en) redka dislipidemija (sl) اعتلال ليبيدات الدم النادر (ar)
name	dislipidemia rara (es) dislipèmia rara (ca) rare dyslipidemia (en) redka dislipidemija (sl) اعتلال ليبيدات الدم النادر (ar)
instance of	wds:Q55785266-F2229834-E782-46C5-A7D2-E4ACA832C3A1
instance of	class of disease
subclass of	wds:Q55785266-3AD6F3C4-33F1-41CF-B27D-08FF21C00904 wds:Q55785266-6ead953b-4373-c48a-aa41-47f435351f7d
subclass of	lipid metabolism disorder rare genetic endocrine disease
Orphanet ID	wds:Q55785266-698E2873-9638-4F1C-9AD6-4E53F9E7E1BE
ICD-10-CM	wds:Q55785266-0F073DBB-C7ED-4E1F-9AC9-E791329EF577 wds:Q55785266-1CA6E278-6991-4F8E-9DA4-9E8A3BD3C798 wds:Q55785266-445ECB90-373F-456A-BF16-4FB1CA6CE8E1 wds:Q55785266-836ADDC2-5253-41D4-8698-958AA97F6E4F wds:Q55785266-9498BFFA-6E72-4E7E-82A1-E46942496C7E wds:Q55785266-A7933724-EDDF-4113-8ECF-A429038902FE wds:Q55785266-E5230CCB-CBE8-48FE-B73A-85AD4573C8D5 wds:Q55785266-FC5DC762-B8F0-411E-B6FE-3AFA543D2BF5 wds:Q55785266-FC81F077-F91C-4461-B1BD-09C1F3EC4095
Orphanet ID	101953
ICD-10-CM	E78.0 E78.9 E78.6 E78.4 E78.2 E78.1 E78.3 E78.5 E78.8
skos:altLabel	rare lipid metabolism disorder (en)
UMLS CUI	wds:Q55785266-019DCDB8-CB1B-44DC-80A8-7EF14CEFA3A2 wds:Q55785266-1B4C6FE3-AF01-4DA1-AE10-4912C1AA922B
UMLS CUI	C0242339 C5681798
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q55785266
is subclass of of	gangliosidosis Desmosterolosis short-chain acyl-coenzyme A dehydrogenase deficiency metachromatic leukodystrophy neutral lipid storage disease lipoid proteinosis hydrops-ectopic calcification-moth-eaten skeletal dysplasia mucosulfatidosis 2,4 Dienoyl-CoA reductase deficiency fatty acid oxidation and ketogenesis disorder with hypertrophic cardiomyopathy syndromic dyslipidemia bile acid synthesis defect with cholestasis and malabsorption sterol metabolism disorder with epilepsy encephalopathy due to prosaposin deficiency congenital ichthyosis-intellectual disability-spastic quadriplegia syndrome disorder of plasmalogens biosynthesis disorder of lipid absorption and transport idiopathic malabsorption due to bile acid synthesis defects fatty acid oxidation and ketogenesis disorder with dilated cardiomyopathy megaconial type congenital muscular dystrophy progressive myoclonic epilepsy type 8 hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency
is subclass of of	wds:Q3335662-E9B6E766-744C-4371-A976-915881B73FC8 wds:Q55784327-149AE5DC-2E58-49A8-99D2-DB688EDEC6D4 wds:Q55787665-D4FBA693-2A8D-4E3A-ACB2-B4D9D509CD74 wds:Q5264836-EE4C8EBA-4438-4E76-A943-479A52D42286 wds:Q55786200-44336C8F-3F91-4C6C-B413-B123DCE2D72C wds:Q55788637-7A054865-50F9-4AE7-9BF2-93F020949451

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