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Cataract 41 (CTRCT41)

Alias:
Ctrct41
Cataract 41, Congenital Nuclear Type
Congenital Nuclear Type Cataract 41
Congenital Nuclear Cataract 41
Cataract, Type 41
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Cataract 41, is also known as ctrct41. An important gene associated with Cataract 41 is WFS1 (Wolframin ER Transmembrane Glycoprotein). Affiliated tissues include eye.
Related ID：
MALACARDS：CTR136
OMIM：116400
MESH：D002386

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Unknown
--
1
8
2
CTR136

Medical Symptom

#
Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

#
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

Title
PMID
Journal
Year
IF
No Data Found!
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