Pathologic Nystagmus

Alias:
Nystagmus
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Pathologic Nystagmus, also known as nystagmus, is related to nystagmus 7, congenital, autosomal dominant and nystagmus 3, congenital, autosomal dominant, and has symptoms including ophthalmoplegia, deficiencies of smooth pursuit movements and neurologic symptoms. An important gene associated with Pathologic Nystagmus is FRMD7 (FERM Domain Containing 7), and among its related pathways/superpathways are Visual Cycle in Retinal Rods and Visual signal transduction: Cones. The drugs Dopamine and Gabapentin have been mentioned in the context of this disorder. Affiliated tissues include eye and brain, and related phenotypes are behavior/neurological and pigmentation
Related ID:
MESH:D009759
ICD11:1029792395

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Unknown
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22
293
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Medical Symptom

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Gene & Mutation

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Disease Model

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MGI
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References Literature

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