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Oligocone Trichromacy

Alias:
Trichromacy, Oligocone
Oligocone Syndrome
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Oligocone Trichromacy, also known as trichromacy, oligocone, is related to pathologic nystagmus and color blindness. An important gene associated with Oligocone Trichromacy is CEP290 (Centrosomal Protein 290). Affiliated tissues include eye and retina, and related phenotypes are abnormal electroretinogram and photophobia
Related ID：
MALACARDS：OLG014

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
AD
Infant
<1/1000000
1
13
--
OLG014

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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