Corneal Dystrophy, Meesmann, 1 (MECD1)

Alias:
Meesmann Corneal Dystrophy
Mecd
Corneal Dystrophy, Meesmann Epithelial
Juvenile Hereditary Epithelial Dystrophy of Meesmann
Corneal Dystrophy, Juvenile Epithelial of Meesmann
Juvenile Hereditary Epithelial Dystrophy
Meesmann Epithelial Corneal Dystrophy
Meesmann Corneal Dystrophy 1
Mecd1
Corneal Dystrophy, Juvenile Epithelial, of Meesmann
Juvenile Epithelial Corneal Dystrophy of Meesmann
Meesmann Corneal Epithelial Dystrophy
Dystrophy, Corneal, Meesmann, Type 1
Corneal Dystrophy, Meesmann 1
Dystrophy, Corneal, Meesmann
Meesman's Corneal Dystrophy
Stocker-Holt Dystrophy
Mcd
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Corneal Dystrophy, Meesmann, 1, also known as meesmann corneal dystrophy, is related to macular dystrophy, corneal and corneal dystrophy, lisch epithelial. An important gene associated with Corneal Dystrophy, Meesmann, 1 is KRT12 (Keratin 12), and among its related pathways/superpathways is Keratinization. Affiliated tissues include eye and smooth muscle, and related phenotypes are photophobia and corneal dystrophy
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Child
<1/1000000
17
83
14

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
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IF
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