Corneal Dystrophy, Lattice Type I (CDL1)

Alias:
Lattice Corneal Dystrophy Type I
Lcd1
Biber-Haab-Dimmer Dystrophy
Classic Lattice Corneal Dystrophy
Lattice Corneal Dystrophy Type 1
Cdl1
Lcdi
Lcd
Dystrophy, Corneal, Lattice Type I
Lattice Corneal Dystrophy, Type I
Corneal Dystrophy, Lattice Type 1
Corneal Dystrophy Lattice Type I
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Corneal Dystrophy, Lattice Type I, also known as lattice corneal dystrophy type i, is related to corneal dystrophy and lattice corneal dystrophy. An important gene associated with Corneal Dystrophy, Lattice Type I is TGFBI (Transforming Growth Factor Beta Induced), and among its related pathways/superpathways is Coregulation of Androgen receptor activity. Affiliated tissues include eye, and related phenotypes are corneal opacity and visual loss
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
All ages
--
3
28
16

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
Year
IF
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