Disease core ontology applied to Rare Diseases

Last uploaded: February 7, 2014
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Preferred Name

Familial long QT syndrome
Synonyms

Congenital long QT syndrome
ID

http://www.limics.org/hrdo/rdfns#pat_id_658
ageOfOnset

Childhood
altLabel

Congenital long QT syndrome
id_Medline

http://www.ncbi.nlm.nih.gov/sites/entrez?Db=pubmed&Cmd=DetailsSearch&Term=jervell+lange+nielsen+syndrome+OR+romano+ward+syndrome+OR+((long+qt+syndrome)+genetic+diseases,+inborn)
id_OMS

I45.8
id_Orpha

768
inheritance

Autosomal dominant

Autosomal recessive
patType

disease
prefixIRI

hrdo:pat_id_658
prefLabel

Familial long QT syndrome
prevalence

Unknown
subClassOf

http://www.limics.org/hrdo/rdfns#typ_id_11
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