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Clinical Disorder Search

Terms: night blindness, jaundice, cataracts, etc.
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Disorder Name Genes Alternate Names OMIM Inheritance
Waardenburg Syndrome, Type 1 PAX3 WS1, Waardenburg syndrome with dystopia canthorum, Klein-Waardenburg syndrome 193500 autosomal dominant
Waardenburg Syndrome, Type 2 SOX10, MITF, SNAI2 Waardenburg syndrome without dystopia canthorum, WS2 193510, 600193, 606662, 608890, 611584, 103470 autosomal dominant
Waardenburg Syndrome, Type 3 PAX3 Klein-Waardenburg syndrome, Waardenburg syndrome with upper limb anomalies 148820 autosomal dominant, autosomal recessive?
Waardenburg Syndrome, Type 4 SOX10, EDNRB Waardenburg-Shah syndrome, WS4, Waardenburg syndrome with Hirschsprung disease 277580, 613265, 613266 autosomal recessive, autosomal dominant
Wagner Syndrome VCAN WGN1, Wagner vitreoretinal degeneration, erosive vitreoretinopathy, ERVR 143200 autosomal dominant
Walker-Warburg Syndrome POMT1, POMT2, POMGNT1, FKTN, FKRP, LARGE COD-MD syndrome, WWS, dystroglycanopathy, MDDG, HARD syndrome, MEB 236670 autosomal recessive
Watson Syndrome NF1 pulmonic stenosis with cafe-au-lait spots 193520 autosomal dominant
Weill-Marchesani Syndrome 1 ADAMTS10 WM syndrome, WMS1, autosomal recessive Weill-Marchesani syndrome 277600 autosomal recessive
Weill-Marchesani Syndrome 2 FBN1 glaucoma-lens ectopia-microspherophakia-stiffness-shortness syndrome, Weill-Marchesani syndrome 2, WMS2, GEMSS 608328 autosomal dominant
Weill-Marchesani-Like Syndrome ADAMTS17 613195 autosomal recessive
Wildervanck Syndrome ? cervicooculoacoustic syndrome 314600 ?
Williams Syndrome ELN WMS, Williams-Beuren syndrome, WBS 194050 deletion syndrome
Wilson Disease ATP7B hepatolenticular degeneration, WD 277900 autosomal recessive
Wolfram Syndrome 1 WFS1 WFS1, WFS, DIDMOAD 222300 autosomal recessive
Wolfram Syndrome 2 CISD2 DIDMOAD, WFS2 604928 autosomal recessive