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Clinical Disorder Search

Terms: night blindness, jaundice, cataracts, etc.
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Disorder Name Genes Alternate Names OMIM Inheritance
Vici Syndrome EPG5 cataract, VICIS, immunodeficiency with cleft lip/palate, hypopigmentation, and absent corpus callosum 242840 autosomal recessive
Vitreoretinal Degeneration, Snowflake Type KCNJ13 snowflake vitreoretinal degeneration, SVD 193230 autosomal dominant
Vitreoretinochoroidopathy BEST1 VRCP, ADVIRC, MRCS, microcornea, posterior staphyloma, rod-cone dystrophy, cataract 193220 autosomal dominant
Vitreoretinopathy with Epiphyseal Dysplasia COL2A1 vitreoretinopathy with phalangeal epiphyseal dysplasia, chondrocalcin 120140 autosomal dominant
Von Hippel-Lindau Syndrome VHL VHL, angiomatosis retinae, VHL syndrome 193300 autosomal dominant