Retinitis Pigmentosa 80 (RP80)

Alias:
Rp80
Retinitis Pigmentosa, Type 80
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Retinitis Pigmentosa 80, also known as rp80, is related to asphyxiating thoracic dystrophy and retinal ciliopathy due to mutation in the retinitis pigmentosa-1 gene. An important gene associated with Retinitis Pigmentosa 80 is IFT140 (Intraflagellar Transport 140). Affiliated tissues include retina and bone, and related phenotypes are global developmental delay and progressive visual loss
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Unknown
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1
8
9

Medical Symptom

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Description
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Gene & Mutation

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Disease Model

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MGI
Related Gene
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Publications
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References Literature

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