Online Mendelian Inheritance in Man

Last uploaded: August 28, 2024

Preferred Name	OCULAR MOTOR APRAXIA
Synonyms	OCULOMOTOR APRAXIA, COGAN TYPE COMA SACCADE INITIATION FAILURE, CONGENITAL
ID	http://purl.bioontology.org/ontology/OMIM/257550
altLabel	OCULOMOTOR APRAXIA, COGAN TYPE COMA SACCADE INITIATION FAILURE, CONGENITAL
cui	C0543874
Gene Locus	2q13
Gene Symbol	COMA
Has manifestation	http://purl.bioontology.org/ontology/OMIM/MTHU053693 http://purl.bioontology.org/ontology/OMIM/MTHU053692
MIMTYPEMEANING	Mendelian phenotype or locus, molecular basis unknown.
notation	257550
OMIM Entry Type	5
OMIM MimType Value	perc
prefLabel	OCULAR MOTOR APRAXIA
Scope Statement	Ocular movement dysfunction improves with age [MISCELLANEOUS]
tui	T047

Delete	Subject	Author	Type	Created
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Mapping To	Ontology	Source
http://purl.bioontology.org/ontology/MDRFRE/10053877	MDRFRE	CUI
http://purl.bioontology.org/ontology/MDRGER/10053941	MDRGER	CUI
http://purl.bioontology.org/ontology/MESH/C537423	MESH	CUI
http://purl.bioontology.org/ontology/SCTSPA/405809000	SCTSPA	CUI
http://purl.bioontology.org/ontology/MDRGER/10053877	MDRGER	CUI
http://purl.bioontology.org/ontology/MEDDRA/10053877	MEDDRA	CUI
http://purl.bioontology.org/ontology/MDRFRE/10053941	MDRFRE	CUI
http://purl.bioontology.org/ontology/SNOMEDCT/405809000	SNOMEDCT	CUI
http://purl.bioontology.org/ontology/MEDDRA/10053941	MEDDRA	CUI
http://purl.bioontology.org/ontology/RCD/Xa867	RCD	CUI