(Q2074059)

English

oculomotor apraxia

The absence or defect of controlled, voluntary, and purposeful eye movement

Cogan’s Ocular Motor Apraxia
Saccadic Initiation Failure
SIF
OMA
Ocular apraxia

In more languages

Statements

class of disease

0 references

eye and adnexa disease

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neuro-ophthalmological disease

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

ocular motility disease

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http://www.orpha.net/ORDO/Orphanet_98688

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Identifiers

PatientsLikeMe condition ID

occular-motor-apraxia

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Human Phenotype Ontology ID

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ICD-11 (foundation)

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ICD-11 ID (MMS)

9C82.4

subject named as

Oculomotor apraxia

0 references

Microsoft Academic ID

0 references

0 references

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mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

Sitelinks

Wikipedia(5 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

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