nemaline myopathy 6, autosomal dominant Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/609273
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Genes

1 genes associated with the nemaline myopathy 6, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
KBTBD13 kelch repeat and BTB (POZ) domain containing 13