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Retinitis Pigmentosa 39 (RP39)

Alias:
Rp39
Retinitis Pigmentosa, Type 39
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Retinitis Pigmentosa 39, also known as rp39, is related to cone-rod dystrophy 1 and retinitis pigmentosa 85. An important gene associated with Retinitis Pigmentosa 39 is USH2A (Usherin), and among its related pathways/superpathways are Joubert syndrome and Ciliopathies. Affiliated tissues include retina and bone, and related phenotypes are visual impairment and abnormal electroretinogram
Related ID：
MALACARDS：RTN141
OMIM：613809
MESH：D012174

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Unknown
--
22
119
152
RTN141

Medical Symptom

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Gene & Mutation

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MGI
Related Gene
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No data available

References Literature

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