about
P279
Autosomal dominant vitreoretinochoroidopathy (ADVIRC).BEST1-related autosomal dominant vitreoretinochoroidopathy: a degenerative disease with a range of developmental ocular anomalies.Mislocalisation of BEST1 in iPSC-derived retinal pigment epithelial cells from a family with autosomal dominant vitreoretinochoroidopathy (ADVIRC)Autosomal dominant vitreoretinochoroidopathy. Report of the third family.Histopathologic study of autosomal dominant vitreoretinochoroidopathy in a 26-year-old woman.Clinical and electrophysiological findings in autosomal dominant vitreoretinochoroidopathy: report of a new pedigree.Mutations of VMD2 splicing regulators cause nanophthalmos and autosomal dominant vitreoretinochoroidopathy (ADVIRC).Histopathologic study of autosomal dominant vitreoretinochoroidopathy. Peripheral annular pigmentary dystrophy of the retina.Long-term changes in autosomal dominant vitreoretinochoroidopathy (ADVIRC).AUTOSOMAL DOMINANT VITREORETINOCHOROIDOPATHY: When Molecular Genetic Testing Helps Clinical Diagnosis.Long-Term Macular Changes in the First Proband of Autosomal Dominant Vitreoretinochoroidopathy (ADVIRC) Due to a Newly Identified Mutation in BEST1.Electro-oculography in autosomal dominant vitreoretinochoroidopathyAutosomal dominant vitreoretinochoroidopathyAutosomal dominant vitreoretinochoroidopathyAutosomal dominant vitreoretinochoroidopathy with normal electrooculogram in a German family
P921
Q33643020-F266454D-DAC6-4C8B-97CE-8B1130ECC212Q35130828-4D055E4F-8818-44FC-9792-1EE282788B8BQ37273988-5D8B462B-9EF4-4304-B1D0-E2CC354E9661Q40874601-11002754-8037-4807-9A80-B9FB9BDC921EQ42474700-2AA9A340-490A-4EB7-A1C1-71014BBD7ADDQ43755544-342EFB34-0888-4A0D-87E1-D6DA7359F5CEQ45081362-06F1BACD-429A-4670-A763-02A7F06E7308Q46591015-D188D240-36F2-4C9C-82DA-6551A07E1ABFQ49631164-48414DB2-6791-478E-BBEB-09DF13FC95FEQ49694273-E0D1F0B9-E3D7-4187-A822-7B2F1F9770AEQ52985164-E618C01F-A774-41E8-AF30-797E904C857BQ67588108-4E553AD6-0DDC-4CED-9474-6F5DC82CAD38Q70304401-ECBF36E1-F0BC-4BB1-9249-D66DDB84E127Q73654684-494540E2-A4D8-4FB5-BEEE-60E339FDE39DQ74301662-B91D561A-520A-4423-A1C6-000199D2EAA0
P921
name
autosomal dominant vitreoretinochoroidopathy
@en
rétino-choroïdopathie vitreuse dominante
@fr
type
label
autosomal dominant vitreoretinochoroidopathy
@en
rétino-choroïdopathie vitreuse dominante
@fr
altLabel
ADVIRC
@en
Microcornea, Rod-Cone Dystrophy, Cataract, and Posterior Staphyloma
@en
VITREORETINOCHOROIDOPATHY
@en
VITREORETINOCHOROIDOPATHY; VRCP
@en
VRCP
@en
Vitreoretinochoroidopathy With Microcornea, Glaucoma, and Cataract
@en
Vitreoretinochoroidopathy, Autosomal Dominant
@en
Vitreoretinochoroidopathy, Autosomal Dominant, With Nanophthalmos
@en
prefLabel
autosomal dominant vitreoretinochoroidopathy
@en
rétino-choroïdopathie vitreuse dominante
@fr
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MONDO:0008662