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Cataract 47 (CTRCT47)

Alias:
Juvenile Cataract-Microcornea-Renal Glucosuria Syndrome
Cataract, Juvenile, with Microcornea and Glucosuria
Ctrct47
Cataract 47, Juvenile, with Microcornea
Cataract, Juvenile, with Microcornea
Cataract, Juvenile, with Microcornea and Glucosuria, Formerly
Juvenile Cataract-Microcornea-Renal Glycosuria Syndrome
Cataract, Type 47, Juvenile, with Microcornea
Cjmg, Formerly
Cjmg
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Cataract 47, is also known as juvenile cataract-microcornea-renal glucosuria syndrome. An important gene associated with Cataract 47 is SLC16A12 (Solute Carrier Family 16 Member 12). Affiliated tissues include eye, and related phenotypes are cataract and microcornea
Related ID：
MALACARDS：CTR162
OMIM：612018
MESH：D002386

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Child
<1/1000000
1
3
4
CTR162

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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