Granular Corneal Dystrophy

Alias:
Familial Hereditary Corneal Degeneration
Corneal Dystrophies, Hereditary
Hereditary Corneal Dystrophy
Granular Dystrophy Corneal
Hereditary Corneal Opacity
Corneal Dystrophy Nos
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Granular Corneal Dystrophy, also known as familial hereditary corneal degeneration, is related to corneal dystrophy, groenouw type i and corneal dystrophy and perceptive deafness. An important gene associated with Granular Corneal Dystrophy is TGFBI (Transforming Growth Factor Beta Induced), and among its related pathways/superpathways are IL-15 Signaling and its Primary Biological Effects in Different Immune Cell Types and Articular Cartilage Extracellular Matrix. The drugs Pharmaceutical Solutions and Hyaluronic acid have been mentioned in the context of this disorder. Affiliated tissues include eye and endothelial, and related phenotype is vision/eye.
Related ID:
MESH:D003317
ICD11:1291475891

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Unknown
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16
115
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Medical Symptom

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Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Related Drugs

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Disease Model

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Name
MGI
Related Gene
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Publications
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References Literature

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