About: autosomal dominant hyperinsulinism due to SUR1 deficiency

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About: autosomal dominant hyperinsulinism due to SUR1 deficiency Goto Sponge NotDistinct Permalink

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

Attributes	Values
rdf:type	Item
exact match	wds:Q56013937-208431E0-C626-4FE4-8B95-7031C6BECA71
exact match	http://www.orpha.net/ORDO/Orphanet_276575
Mondo ID	wds:Q56013937-4F17D1C1-FCE1-403E-8A9D-76445623E707
Mondo ID	http://purl.obolibrary.org/obo/MONDO_0017184
Mondo ID	MONDO_0017184
rdfs:label	autosomal dominant hyperinsulinism due to SUR1 deficiency (en)
skos:prefLabel	autosomal dominant hyperinsulinism due to SUR1 deficiency (en)
name	autosomal dominant hyperinsulinism due to SUR1 deficiency (en)
instance of	wds:Q56013937-C7DA7816-43D1-4B3F-A517-177DA8E5336D
instance of	class of disease
Orphanet ID	wds:Q56013937-7F3D062A-5A8A-4A90-9983-F24573B37A5B
genetic association	wds:Q56013937-4C2EBBD7-1697-4D15-9B59-FD1960BDC8D9
ICD-10-CM	wds:Q56013937-B428251D-13DF-46C9-9086-EE5757D02348
Orphanet ID	276575
genetic association	ABCC8
ICD-10-CM	E16.1
skos:altLabel	Autosomal dominant hyperinsulinemic hypoglycemia due to SUR1 deficiency (en)
UMLS CUI	wds:Q56013937-DEE88D4D-CF68-4C45-8E0C-5E19A9CB0EE6
UMLS CUI	C4274080
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q56013937
is genetic association of	ABCC8
is genetic association of	wds:Q18031792-EB00BDCC-88C0-4881-9F0F-15A4B2A8CA14

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