Matches in DBpedia 2014 for { <http://dbpedia.org/resource/Erondu–Cymet_syndrome> ?p ?o. }
Showing items 1 to 11 of
11
with 100 items per page.
- Erondu–Cymet_syndrome 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.".
- Erondu–Cymet_syndrome wikiPageID "20733310".
- Erondu–Cymet_syndrome wikiPageRevisionID "569356263".
- Erondu–Cymet_syndrome subject Category:Genetic_disorders_with_no_OMIM.
- Erondu–Cymet_syndrome subject Category:Syndromes.
- Erondu–Cymet_syndrome 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 label "Erondu–Cymet syndrome".
- Erondu–Cymet_syndrome sameAs Erondu%E2%80%93Cymet_syndrome.
- Erondu–Cymet_syndrome sameAs Q5395327.
- Erondu–Cymet_syndrome sameAs Q5395327.
- Erondu–Cymet_syndrome wasDerivedFrom Erondu–Cymet_syndrome?oldid=569356263.