Occult Macular Dystrophy (OCMD)

Alias:
Ocmd
Omd
Dystrophy, Macular, Occult
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Occult Macular Dystrophy, also known as ocmd, is related to severe early-childhood-onset retinal dystrophy and retinitis pigmentosa 1. An important gene associated with Occult Macular Dystrophy is RP1L1 (RP1 Like 1), and among its related pathways/superpathways are Ciliopathies and Visual signal transduction: Cones. Affiliated tissues include retina and eye, and related phenotypes are macular dystrophy and slow decrease in visual acuity
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
All ages
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14
88
12

Medical Symptom

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Description
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HPO Source Accession
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Gene & Mutation

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Related Drugs

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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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