Vitreoretinochoroidopathy (VRCP)

Alias:

Autosomal Dominant Vitreoretinochoroidopathy

Advirc

Microcornea, Rod-Cone Dystrophy, Cataract, and Posterior Staphyloma 2

Vitreoretinochoroidopathy with Microcornea, Glaucoma, and Cataract

Vitreoretinochoroidopathy, Autosomal Dominant, with Nanophthalmos

Vitreoretinochoroidopathy Dominant

Vitreoretinochoroidopathy, Autosomal Dominant

Vrcp

Vitreoretinochoroidopathy Autosomal Dominant with Nanophthalmos, Microcornea, Rod-Cone Dystrophy, Cataract and Posterior Staphyloma

Vitreoretinochoroidopathy with Microcornea-Glaucoma-Cataract

Vrcp Autosomal Dominant

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Vitreoretinochoroidopathy, also known as autosomal dominant vitreoretinochoroidopathy, is related to macular retinal edema and macular dystrophy, dominant cystoid. An important gene associated with Vitreoretinochoroidopathy is BEST1 (Bestrophin 1), and among its related pathways/superpathways are Transport of inorganic cations/anions and amino acids/oligopeptides and Ion channel transport. Affiliated tissues include eye and retina, and related phenotypes are microphthalmia and dyschromatopsia

Related ID：

MALACARDS：VTR010

OMIM：193220

MESH：C536352