About: Pseudohyperaldosteronism type 2

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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) хвороба людини (uk)
exact match	wds:Q55783401-8BD0C686-B143-4731-A40C-3C9505D71F8E
exact match	http://www.orpha.net/ORDO/Orphanet_88660
Mondo ID	wds:Q55783401-04559B3A-0017-4467-A4A8-F8D8A2CB6CF0
Mondo ID	http://purl.obolibrary.org/obo/MONDO_0011517
Mondo ID	MONDO_0011517
rdfs:label	Pseudohyperaldosteronism type 2 (en) Pseudohyperaldosteronismus Typ 2 (de) pseudo-hyperaldosteronisme type 2 (fr)
skos:prefLabel	Pseudohyperaldosteronism type 2 (en) Pseudohyperaldosteronismus Typ 2 (de) pseudo-hyperaldosteronisme type 2 (fr)
name	Pseudohyperaldosteronism type 2 (en) Pseudohyperaldosteronismus Typ 2 (de) pseudo-hyperaldosteronisme type 2 (fr)
instance of	wds:Q55783401-6315CB57-10CA-4191-8726-6752BBA7585B wds:Q55783401-A46ABFFF-9E32-4C7E-A0F9-472BEF94B157
instance of	class of disease rare disease
subclass of	wds:Q55783401-00de1f8c-428a-613c-2bb2-2ed3980ff4f4 wds:Q55783401-290D7740-1FEB-43F4-8621-99D0ECAA55F6 wds:Q55783401-30FCDF43-8E54-4752-9F96-7492EE9BBF14 wds:Q55783401-6DD44B4C-3122-43B4-8C4B-4113AAD51407 wds:Q55783401-E5DC4CA3-7111-4F75-8886-69E550DE0FBC
subclass of	pseudohyperaldosteronism gestational hypertension rare genetic gynecological and obstetrical diseases complication of pregnancy, childbirth and the puerperium genetic hypertension
Google Knowledge Graph ID	wds:Q55783401-DA45A9CE-E565-473F-994D-EDC3BC2732B1
KEGG ID	wds:Q55783401-34A5DEE6-4C05-40F6-B848-ACF9B4B336E7
Google Knowledge Graph ID	http://g.co/kg/g/11hcw7vvkq
KEGG ID	http://www.kegg.jp/entry/H00603
Google Knowledge Graph ID	/g/11hcw7vvkq
KEGG ID	H00603
Orphanet ID	wds:Q55783401-2A88CC84-1959-407C-AA43-6192BFB3FB3A
genetic association	wds:Q55783401-D00727F9-B4C0-4581-A3D0-3937891FDBEB
ICD-10-CM	wds:Q55783401-8CBB5763-ECE9-4520-B8C8-28DB340CAF36
OMIM ID	wds:Q55783401-6D95B346-B100-4131-9D30-4FFF6B506D31
Orphanet ID	88660
genetic association	NR3C2
ICD-10-CM	I15.1
OMIM ID	605115
skos:altLabel	Early-onset hypertension with exacerbation in pregnancy (en) Hypertension due to gain-of-function mutations in the mineralocorticoid receptor (en) HYPERTENSION, EARLY-ONSET, AUTOSOMAL DOMINANT, WITH SEVERE EXACERBATION IN PREGNANCY (en)
UMLS CUI	wds:Q55783401-226199F0-2BC9-44D7-9E14-9935685A017B wds:Q55783401-3006542C-35C4-40BA-A00B-DF26C5C91312
MeSH descriptor ID	wds:Q55783401-6E674939-30D1-4885-8B85-87509D76A2F1
ICD-11 (foundation)	wds:Q55783401-abefc475-41fc-b5c0-78d6-60253d920a23
MeSH descriptor ID	http://id.nlm.nih.gov/mesh/C565359
UMLS CUI	C1854631 C4707886
MeSH descriptor ID	C565359
ICD-11 (foundation)	538048714
is owl:sameAs of	Pseudohyperaldosteronism type 2
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q55783401 https://de.wikipedia.org/wiki/Pseudohyperaldosteronismus_Typ_2

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