Retinal Perforation

Alias:
Retinal Perforations
Retinal Break
Retinal Break Nos
Retinal Dialysis
Ruptured Retina
Retinal Tear
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Retinal Perforation, also known as retinal break, is related to macular dystrophy, dominant cystoid and degenerative myopia. An important gene associated with Retinal Perforation is COL2A1 (Collagen Type II Alpha 1 Chain), and among its related pathways/superpathways are ERK Signaling and Signal Transduction. The drugs Midazolam and Fentanyl have been mentioned in the context of this disorder. Affiliated tissues include retina and eye, and related phenotypes are Increased gamma-H2AX phosphorylation and nervous system
Related ID:
MESH:D012167
ICD11:236011795

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Unknown
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21
170
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Medical Symptom

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Description
HPO Frequency
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No data available

Gene & Mutation

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Disease Model

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MGI
Related Gene
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Publications
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References Literature

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