Disease core ontology applied to Rare Diseases

Last uploaded: February 7, 2014
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Preferred Name

Caffey disease
Synonyms

Infantile Cortical Hyperostosis
ID

http://www.limics.org/hrdo/rdfns#pat_id_431
ageOfOnset

Neonatal/infancy
altLabel

Infantile Cortical Hyperostosis
id_Medline

http://www.ncbi.nlm.nih.gov/sites/entrez?Db=pubmed&Cmd=Search&Term=Caffey+dis*%5Bti%5D+OR+Caffey%27s%5Bti%5D+OR+infantile+cortical+hyperostosis%5Btw%5D+OR+Hyperostosis%2C+Cortical%2C+Congenital%5Bmh%5D
id_MIM

114000
id_OMS

M89.8
id_Orpha

1310
inheritance

Autosomal dominant
patType

malformation syndrome
prefixIRI

hrdo:pat_id_431
prefLabel

Caffey disease
prevalence

Unknown
subClassOf

http://www.limics.org/hrdo/rdfns#typ_id_8
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