Otitis Media (OMS)

Alias:
Opsoclonus-Myoclonus Syndrome
Otitis Media, Susceptibility to
Oms
Kinsbourne Syndrome
Paraneoplastic Opsoclonus-Myoclonus-Ataxia Syndrome
Opsoclonus-Myoclonus-Ataxia Syndrome
Paraneoplastic Opsoclonus-Myoclonus
Dancing Eye-Dancing Feet Syndrome
Otitis Media, Chronic/recurrent
Ataxo-Opso-Myoclonus Syndrome
Dancing Eye Syndrome
Poma Syndrome
Oma Syndrome
Come/rom
{otitis Media, Susceptibility to}
Infectious Otitis Media
Opsoclonus Myoclonus
Om
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Otitis Media, also known as opsoclonus-myoclonus syndrome, is related to suppurative otitis media and chronic purulent otitis media, and has symptoms including myoclonus and ophthalmoplegia. An important gene associated with Otitis Media is A2ML1 (Alpha-2-Macroglobulin Like 1), and among its related pathways/superpathways are Innate Immune System and IL-1 Family Signaling Pathways. The drugs Ketorolac and Sodium citrate have been mentioned in the context of this disorder. Affiliated tissues include eye and breast, and related phenotypes are ataxia and myoclonus
Related ID:
MESH:D010033
ICD11:1079654421

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Infant
<1/1000000
54
513
9

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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