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GENE -- gene symbol (links to gene page)Condition -- named syndrome or disease+ -- predominantly adult-onset; pediatric cases documented
B16 entries · 5 genes, 11 conditions
Gene Symbols (5)
BAG3BCS1LBICD2BIN1BSCL2
Conditions (11)
Barth syndromeBatten disease (CLN3)Becker muscular dystrophyBecker myotonia congenitaBehr syndromeBethlem myopathyBrown-Vialetto-van Laere syndromeBone Morphogenetic ProteinsBrachial Plexus: StructureBrachioradial PruritisBulbo-Spinal Muscular Atrophy (SMAX1; BSMA; SBMA; Kennedy Syndrome)

Data sourced from the Washington University Neuromuscular Disease Center, NCBI Gene, and OMIM. For clinical use, always refer to primary sources.