About: Erondu–Cymet syndrome

An Entity of Type: disease, from Named Graph: http://dbpedia.org, within Data Space: dbpedia.org

Erondu–Cymet syndrome is a syndrome caused by a translocation on the 21st chromosome. The genetic karyotype for people with this condition is 46, XY, inv(21)(q11.2q22.1). Findings in these patients include hypotension, hypoxemia, seizures, and impairment of cognitive ability. Patients with this condition may have persistent left superior vena cava that drains into the left atrium, as well as pulmonary arteriovenous malformations. Erondu–Cymet syndrome was discovered in 2006 by Ugochi Erondu and Tyler Cymet.

Property	Value
dbo:abstract	Erondu–Cymet syndrome is a syndrome caused by a translocation on the 21st chromosome. The genetic karyotype for people with this condition is 46, XY, inv(21)(q11.2q22.1). Findings in these patients include hypotension, hypoxemia, seizures, and impairment of cognitive ability. Patients with this condition may have persistent left superior vena cava that drains into the left atrium, as well as pulmonary arteriovenous malformations. Erondu–Cymet syndrome was discovered in 2006 by Ugochi Erondu and Tyler Cymet. (en)
dbo:wikiPageID	20733310 (xsd:integer)
dbo:wikiPageLength	1233 (xsd:nonNegativeInteger)
dbo:wikiPageRevisionID	1124679999 (xsd:integer)
dbo:wikiPageWikiLink	dbr:Hypoxemia dbr:Tyler_Cymet dbr:Left_atrium dbr:Arteriovenous_malformations dbr:Karyotype dbc:Genetic_disorders_with_no_OMIM dbr:Chromosomal_translocation dbr:Hypotension dbc:Syndromes dbr:Cognition dbr:Seizure dbr:Chromosome_21_(human) dbr:Superior_vena_cava dbr:Trisomy_21
dbp:wikiPageUsesTemplate	dbt:Genetic-disorder-stub dbt:Reflist dbt:Short_description
dcterms:subject	dbc:Genetic_disorders_with_no_OMIM dbc:Syndromes
gold:hypernym	dbr:Syndrome
rdf:type	yago:Abstraction100002137 yago:Attribute100024264 yago:Cognition100023271 yago:Complex105870365 yago:Concept105835747 yago:Condition113920835 yago:Content105809192 yago:Disease114070360 yago:GeneticDisease114151139 yago:Idea105833840 yago:IllHealth114052046 yago:Illness114061805 yago:PathologicalState114051917 yago:PhysicalCondition114034177 yago:PsychologicalFeature100023100 yago:WikicatGeneticDisordersWithNoOMIM dbo:Disease yago:State100024720 yago:Syndrome105870790 yago:Whole105869584 yago:WikicatSyndromes
rdfs:comment	Erondu–Cymet syndrome is a syndrome caused by a translocation on the 21st chromosome. The genetic karyotype for people with this condition is 46, XY, inv(21)(q11.2q22.1). Findings in these patients include hypotension, hypoxemia, seizures, and impairment of cognitive ability. Patients with this condition may have persistent left superior vena cava that drains into the left atrium, as well as pulmonary arteriovenous malformations. Erondu–Cymet syndrome was discovered in 2006 by Ugochi Erondu and Tyler Cymet. (en)
rdfs:label	Erondu–Cymet syndrome (en)
owl:sameAs	freebase:Erondu–Cymet syndrome wikidata:Erondu–Cymet syndrome http://bs.dbpedia.org/resource/Erondu–Cymetov_sindrom https://global.dbpedia.org/id/4jo3n
prov:wasDerivedFrom	wikipedia-en:Erondu–Cymet_syndrome?oldid=1124679999&ns=0
foaf:isPrimaryTopicOf	wikipedia-en:Erondu–Cymet_syndrome
is dbo:wikiPageRedirects of	dbr:Erondu-Cymet_Syndrome dbr:Erondu-Cymet_syndrome
is dbo:wikiPageWikiLink of	dbr:Tyler_Cymet dbr:Erondu-Cymet_Syndrome dbr:Erondu-Cymet_syndrome dbr:Nova_Southeastern_College_of_Osteopathic_Medicine dbr:Chromosome_21 dbr:List_of_syndromes
is foaf:primaryTopic of	wikipedia-en:Erondu–Cymet_syndrome