Retinitis Pigmentosa 86 (RP86)

Alias:
Rp86
Retinitis Pigmentosa, Type 86
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Retinitis Pigmentosa 86, also known as rp86, is related to fundus albipunctatus and congenital stationary night blindness. An important gene associated with Retinitis Pigmentosa 86 is KIAA1549 (KIAA1549). Affiliated tissues include bone and retina, and related phenotypes are progressive visual loss and nyctalopia
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Unknown
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7
33
1

Medical Symptom

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Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
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Gene & Mutation

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Mutations
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Related Drugs

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No data available

Disease Model

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Name
MGI
Related Gene
Strain of Origin
Publications
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References Literature

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PMID
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IF
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