About: OHVIRA

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

medical condition

Attributes	Values
rdf:type	Item
description	medical condition (en) Fehlbildungssyndrom (de) медичний стан (uk) انسداد نصفي مهبلي مع شذوذ كلوي بنفس الجانب (ar)
Mondo ID	wds:Q28439901-015F6D2E-579C-4A32-8C3A-59C048506FBF
Mondo ID	http://purl.obolibrary.org/obo/MONDO_0008636
Mondo ID	MONDO_0008636
rdfs:label	Syndrome d'utérus double-hémivagin-agénésie rénale (fr) OHVIRA (en) OHVIRA-Syndrom (de) متلازمة هرلين-ويرنر-وندرليش (ar)
skos:prefLabel	Syndrome d'utérus double-hémivagin-agénésie rénale (fr) OHVIRA (en) OHVIRA-Syndrom (de) متلازمة هرلين-ويرنر-وندرليش (ar)
name	Syndrome d'utérus double-hémivagin-agénésie rénale (fr) OHVIRA (en) OHVIRA-Syndrom (de) متلازمة هرلين-ويرنر-وندرليش (ar)
instance of	wds:Q28439901-35C5DEE2-CD18-4738-BD63-442E751F5DF1 wds:Q28439901-84B24FE9-44D5-45FE-B885-0719012075AE
instance of	class of disease developmental defect during embryogenesis
subclass of	wds:Q28439901-2D101E7D-FC7E-412A-9938-93AF0F76906B wds:Q28439901-5bc01f92-4f7d-6947-ab80-d59d4c7740c2 wds:Q28439901-70e97c94-4d45-9c26-4020-47ab34f8549a wds:Q28439901-92991C20-34C8-403B-AC5B-CC51622CA7E8 wds:Q28439901-DBACA09A-96B9-4FED-85DD-45B26061123D wds:Q28439901-F449966A-ED83-47A2-A6CF-A4C5E707646C
subclass of	renal agenesis rare genetic gynecological and obstetrical diseases uterine disease syndromic urogenital tract malformation syndromic renal or urinary tract malformation syndromic uterovaginal malformation
Orphanet ID	wds:Q28439901-3b68c983-4d50-ef55-9bb9-969556c3aded
GARD rare disease ID	wds:Q28439901-00cff2d9-4433-8a79-1a3e-afff708e4f76
OMIM ID	wds:Q28439901-394976f1-454a-dad4-b1d6-095646be38ac
Orphanet ID	3411
GARD rare disease ID	1910
OMIM ID	192050
skos:altLabel	UTERUS BICORNIS BICOLLIS WITH PARTIAL VAGINAL SEPTUM AND UNILATERAL HEMATOCOLPOS WITH IPSILATERAL RENAL AGENESIS (en) Double uterus and obstructed hemivagina syndrome (en) Herlyn-Werner syndrome (en) Herlyn-Werner-Wunderlich syndrome (en) OHVIRA syndrome (en) Syndrome OHVIRA (fr) Wunderlich syndrome (en) Obstructed hemivagina and ipsilateral renal anomaly (en)
UMLS CUI	wds:Q28439901-0F531BA4-7798-45E8-A2AF-BB5D4E85CF72 wds:Q28439901-EE7A02C0-8A18-4152-B4AC-B3B2D3008234
MeSH descriptor ID	wds:Q28439901-D3F91DC7-C1B6-4ED6-99F4-B3DA4EE7DBFA
MeSH descriptor ID	http://id.nlm.nih.gov/mesh/C566010
UMLS CUI	C1860549 C4302552
MeSH descriptor ID	C566010
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q28439901 OHVIRA https://de.wikipedia.org/wiki/OHVIRA-Syndrom https://ar.wikipedia.org/wiki/%D9%85%D8%AA%D9%84%D8%A7%D8%B2%D9%85%D8%A9_%D9%87%D8%B1%D9%84%D9%8A%D9%86-%D9%88%D9%8A%D8%B1%D9%86%D8%B1-%D9%88%D9%86%D8%AF%D8%B1%D9%84%D9%8A%D8%B4
is main subject of	Herlyn-Werner-Wunderlich syndrome: An unusual presentation with pyocolpos Spontaneous Cervicovaginal Fistula in OHVIRA Syndrome: a Case Report
is main subject of	wds:Q40100998-73aab47e-4009-9a87-abf9-c4bc66e373b2 wds:Q101216400-b38140c9-499c-676b-f4d1-7c0e52922508

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