About: bilirubin metabolic disorder

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inherited metabolic disorder that involves elevated levels of bilirubin resulting from disruption of bilirubin metabolism

Attributes	Values
rdf:type	Item
owl:sameAs	bilirubin metabolic disorder
description	Krankheit (de) хвороба (uk) gruppo di malattie metaboliche in cui il tratto distintivo, ovvero l'iperbilirubinemia, è dovuto a cause genetiche (it) inherited metabolic disorder that involves elevated levels of bilirubin resulting from disruption of bilirubin metabolism (en)
exact match	wds:Q390475-6B0B1D7C-9B94-45B8-AD28-930FA4BB73EB wds:Q390475-FFDD0B59-2ACB-4C20-A083-C1EBDB8225B0
exact match	http://purl.obolibrary.org/obo/DOID_2741 http://identifiers.org/doid/DOID:2741
health specialty	wds:Q390475-D1ED03A2-1505-49C8-AABF-3BD978E1E18F
drug or therapy used for treatment	wds:Q390475-554281A0-DFF8-4BE8-BFB1-A1BCB031BF24 wds:Q390475-8BD18806-E553-4C29-BF02-7B2FCBCC85D3
ICD-10	wds:q390475-2F465D3B-7B7F-4586-AC00-5E771EB387F1 wds:q390475-7ABB050A-BAEF-4D8C-8184-9A1C83D25201
Disease Ontology ID	wds:Q390475-B75AC3B2-4956-4300-81DF-05BA8604B0C3
Disease Ontology ID	http://purl.obolibrary.org/obo/DOID_DOID:2741
health specialty	endocrinology
drug or therapy used for treatment	phenobarbital
ICD-10	E80.4 E80.6
Disease Ontology ID	DOID:2741
rdfs:label	anhwylder metabolig bilirwbin (cy) bilirubin metabolic disorder (en) forstyrring i bilirubinmetabolismen (nn) hyperbilirubinémie héréditaire (fr) iperbilirubinemie ereditarie (it) motnja presnove bilirubina (sl) trastorn metabòlic de la bilirubina (ca) trastorno metabólico de la bilirrubina (es)
skos:prefLabel	anhwylder metabolig bilirwbin (cy) bilirubin metabolic disorder (en) forstyrring i bilirubinmetabolismen (nn) hyperbilirubinémie héréditaire (fr) iperbilirubinemie ereditarie (it) motnja presnove bilirubina (sl) trastorn metabòlic de la bilirubina (ca) trastorno metabólico de la bilirrubina (es)
name	anhwylder metabolig bilirwbin (cy) bilirubin metabolic disorder (en) forstyrring i bilirubinmetabolismen (nn) hyperbilirubinémie héréditaire (fr) iperbilirubinemie ereditarie (it) motnja presnove bilirubina (sl) trastorn metabòlic de la bilirubina (ca) trastorno metabólico de la bilirrubina (es)
instance of	wds:Q390475-5C49F15F-7D68-404E-8D7F-58599BA44475
instance of	class of disease
subclass of	wds:Q390475-DB62FB10-B0DA-42EC-8521-E6E9FB0526BB wds:Q390475-f85c9bfa-4577-31ae-580e-3f07109ea4f9
subclass of	inherited metabolic disorder hyperbilirubinemia
eMedicine ID	wds:q390475-0909EFBA-46BF-4FE7-BD75-B890570B1183
eMedicine ID	178841
KEGG ID	wds:Q390475-C4A21C24-B1E1-4B2E-866D-611F8A6416BB
KEGG ID	http://www.kegg.jp/entry/H00208
KEGG ID	H00208
ICD-9 ID	wds:q390475-FF53E6C5-F32A-40E3-B18C-8B469D4AB89D
ICD-9 ID	277.4
skos:altLabel	hereditary hyperbilirubinemia (en) hyperbilirubinaemia (en) hyperbilirubinemia (en) trastorn del metabolisme de la bilirubina (ca) trastorno del metabolismo de la bilirrubina (es)
NCI Thesaurus ID	wds:Q390475-72F7D979-2C35-4052-9CC5-60A477D5A966
UMLS CUI	wds:Q390475-29AACB8E-6080-4005-9EAD-B04914C2C62B wds:Q390475-E6E19B34-7759-48D2-80F8-FBD55978339A
MeSH descriptor ID	wds:Q390475-A0AFBF58-8852-4482-BD11-BA811126CFBE
on focus list of Wikimedia project	wds:Q390475-AF98B94B-647C-4EE2-BBBB-33C8F03BD861
Microsoft Academic ID	wds:Q390475-F28B00EB-0A39-4504-860E-E223DE130F27
MeSH tree code	wds:Q390475-078B0875-A72E-4B3B-8413-059A1C0054A3 wds:Q390475-B0847ABF-92E6-475D-B7EB-6B9F3DFAD516
MeSH descriptor ID	http://id.nlm.nih.gov/mesh/D006933
Microsoft Academic ID	https://makg.org/entity/2778814936
MeSH tree code	http://id.nlm.nih.gov/mesh/C16.320.565.300 http://id.nlm.nih.gov/mesh/C18.452.648.300
NCI Thesaurus ID	C84761
UMLS CUI	C0020433 C0020435
MeSH descriptor ID	D006933
on focus list of Wikimedia project	WikiProject Medicine
Microsoft Academic ID	2778814936
MeSH tree code	C16.320.565.300 C18.452.648.300
is about of	bilirubin metabolic disorder https://www.wikidata.org/wiki/Special:EntityData/Q390475 Hereditary hyperbilirubinemia https://it.wikipedia.org/wiki/Iperbilirubinemie_ereditarie
is subclass of of	Dubin-Johnson syndrome Rotor syndrome Gilbert syndrome Crigler-Najjar syndrome primary shunt hyperbilirubinemia
is subclass of of	wds:Q752216-DB2D7565-AC8A-4168-A815-12ADA1CB246F wds:Q1140000-C8EDE978-0BBB-4FBD-83FD-934CBFD07AA9 wds:Q1512812-d316f728-418a-6bd0-21ed-afa2145b9e95 wds:Q1263039-A508C1D1-7730-48FB-B7E2-D283F9FD69CE wds:Q55998622-eb9ddb0d-470c-7ff0-a072-023a7dd7877e
is main subject of	Evaluation and treatment of neonatal hyperbilirubinemia Glucose-6-phosphate dehydrogenase deficiency, the UDP-glucuronosyl transferase 1A1 gene, and neonatal hyperbilirubinemia

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