Schnyder Corneal Dystrophy (SCCD)

Alias:
Schnyder Crystalline Corneal Dystrophy
Sccd
Hereditary Crystalline Stromal Dystrophy of Schnyder
Corneal Dystrophy, Crystalline, of Schnyder
Crystalline Stromal Dystrophy
Scd
Schnyder Crystalline Dystrophy Sine Crystals
Corneal Dystrophy, Schnyder Type
Corneal Dystrophy Crystalline of Schnyder
Dystrophy, Corneal, Crystalline, Schnyder
Corneal Dystrophy, Schnyder
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Schnyder Corneal Dystrophy, also known as schnyder crystalline corneal dystrophy, is related to corneal dystrophy and corneal dystrophy, posterior polymorphous, 3. An important gene associated with Schnyder Corneal Dystrophy is UBIAD1 (UbiA Prenyltransferase Domain Containing 1), and among its related pathways/superpathways are Transport of inorganic cations/anions and amino acids/oligopeptides and Cardiac conduction. Affiliated tissues include eye and skin, and related phenotypes are corneal dystrophy and crystalline corneal dystrophy
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
All ages
<1/1000000
18
98
17

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

Name
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
Journal
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IF
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