Retinitis Pigmentosa 69 (RP69)

Alias:
Rp69
Retinitis Pigmentosa, Type 69
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Retinitis Pigmentosa 69, also known as rp69, is related to bardet-biedl syndrome 16 and joubert syndrome 5. An important gene associated with Retinitis Pigmentosa 69 is KIZ (Kizuna Centrosomal Protein), and among its related pathways/superpathways are Ciliopathies and Joubert syndrome. Affiliated tissues include retina and eye, and related phenotypes are nyctalopia and rod-cone dystrophy
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Unknown
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8
44
5

Medical Symptom

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Description
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Gene & Mutation

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Disease Model

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MGI
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Publications
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References Literature

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