Disease core ontology applied to Rare Diseases

Last uploaded: February 7, 2014

Preferred Name	Ocular motor apraxia, Cogan type
Synonyms
ID	http://www.limics.org/hrdo/rdfns#pat_id_1404
ageOfOnset	Childhood
id_Medline	http://www.ncbi.nlm.nih.gov/sites/entrez?Db=pubmed&Cmd=Search&Term=%28congenital+ocular+motor+apraxia+OR+oculomotor+apraxia%29+AND+cogan
id_MIM	257550
id_OMS	H51.8
id_Orpha	1125
inheritance	Autosomal recessive
patType	disease
prefixIRI	hrdo:pat_id_1404
prefLabel	Ocular motor apraxia, Cogan type
prevalence	<1 / 1 000 000
subClassOf	http://www.limics.org/hrdo/rdfns#typ_id_11

Delete	Subject	Author	Type	Created
No notes to display

Mapping To	Ontology	Source
http://purl.obolibrary.org/obo/MONDO_0009764	CCONT	LOOM
http://purl.obolibrary.org/obo/MONDO_0009764	MONDO	LOOM
http://purl.obolibrary.org/obo/MONDO_0009764	EFO	LOOM
http://purl.obolibrary.org/obo/MONDO_0009764	DOVES	LOOM
http://purl.bioontology.org/ontology/SNOMEDCT/405809000	SNOMEDCT	LOOM
http://purl.obolibrary.org/obo/DOID_0080849	DOID	LOOM
http://purl.obolibrary.org/obo/DOID_0080849	HHEAR	LOOM
http://purl.obolibrary.org/obo/DOID_0080849	DDSS	LOOM
http://purl.obolibrary.org/obo/DOID_0080849	NIFSTD	LOOM
http://purl.obolibrary.org/obo/DOID_0080849	MIDO	LOOM
http://purl.obolibrary.org/obo/DOID_0080849	FNS-H	LOOM
http://www.orpha.net/ORDO/Orphanet_1125	ORDO	LOOM