Ocular Motor Apraxia (COMA)

Alias:
Coma
Oculomotor Apraxia, Congenital, Cogan-Type
Cogan-Type Congenital Oculomotor Apraxia
Saccade Initiation Failure, Congenital
Oculomotor Apraxia, Cogan Type
Oculomotor Apraxia
Comatose
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Ocular Motor Apraxia, also known as coma, is related to oculomotor apraxia and juvenile nephronophthisis, and has symptoms including back pain, dizziness and headache. An important gene associated with Ocular Motor Apraxia is COMA (Cogan-Type Congential Oculomotor Apraxia). The drugs Cangrelor and Ticagrelor have been mentioned in the context of this disorder. Affiliated tissues include brain and eye, and related phenotypes are nephronophthisis and oculomotor apraxia

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Unknown
--
3
16
15

Medical Symptom

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Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Gene
Function
Score
Mutations
No data available

Related Drugs

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CAS Number
Status
Phase
No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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PMID
Journal
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IF
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