Eyelid Disease

Alias:
Eyelid Diseases
Eyelid Disorders
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Eyelid Disease, also known as eyelid disorders, is related to blepharophimosis and familial isolated trichomegaly, and has symptoms including eye manifestations, lid retraction or lag and eyelid pain. An important gene associated with Eyelid Disease is FOXL2 (Forkhead Box L2), and among its related pathways/superpathways are Cohesin complex - Cornelia de Lange syndrome and Prostaglandin 2 biosynthesis and metabolism FM. The drugs Acetylcholine and Mineral oil have been mentioned in the context of this disorder. Affiliated tissues include eye and skin, and related phenotypes are homeostasis/metabolism and growth/size/body region
Related ID:
MESH:D005141
ICD11:136743240/other

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Unknown
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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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