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Optic Atrophy 13 with Retinal and Foveal Abnormalities (OPA13)

Alias:
Opa13
Optic Atrophy with Negative Electroretinograms, Formerly
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Optic Atrophy 13 with Retinal and Foveal Abnormalities, is also known as opa13. An important gene associated with Optic Atrophy 13 with Retinal and Foveal Abnormalities is SSBP1 (Single Stranded DNA Binding Protein 1). Affiliated tissues include retina.
Related ID：
MALACARDS：OPT079
OMIM：165510
MESH：D015418

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Unknown
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1
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4
OPT079

Medical Symptom

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HPO Frequency
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Gene & Mutation

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MGI
Related Gene
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Publications
No data available

References Literature

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