Cataract 18 (CTRCT18)

Alias:
Cataract, Autosomal Recessive Congenital 2
Ctrct18
Catc2
Autosomal Recessive Congenital Cataract 2
Cataract 18, Autosomal Recessive
Cataract 18 Autosomal Recessive
Cataract, Type 18
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Cataract 18, also known as cataract, autosomal recessive congenital 2, is related to cataract and deprivation amblyopia. An important gene associated with Cataract 18 is FYCO1 (FYVE And Coiled-Coil Domain Autophagy Adaptor 1). Affiliated tissues include eye, and related phenotype is nuclear cataract.
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Unknown
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9
33
5

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
Journal
Year
IF
No Data Found!
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