Neuromuscular HOMEepAGE
neuromuscular.wustl.edu
/
A–Z
Home/Browse/O
ABCDEFGHIJKLMNOPQRSTUVWXYZA-Z Index
GENE -- gene symbol (links to gene page)Condition -- named syndrome or disease+ -- predominantly adult-onset; pediatric cases documented
O9 entries · 2 genes, 7 conditions
Gene Symbols (2)
OPA1ORAI1
Conditions (7)
Oculopharyngeal MD (OPMD)†Oculopharyngeal MD (OPMD)\u2020Oculopharyngeal Muscular Dystrophy (OPMD)Oculopharyngeal Myopathy with Leukodystrophy (OPML1)Oculopharyngodistal Myopathies (OPDM)Other Muscle FeaturesOVERVIEW

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