| Disease Aliases (32) | Cnbp myotonic dystrophy Dm2 Dystrophia myotonica 2 Disorder, myotonic Disorders, myotonic Dystrophia myotonica type 2 Eulenburg disease Eulenburg's disease Myotonic myopathy, proximal Myopathies, myotonic Myopathy, myotonic Myotonia fluctuans Myotonic disorder Myotonic disorders Myotonic myopathies Myotonic myopathy Promm Proximal myotonic myopathy Paralysis periodica paramyotonia Paramyotonia congenita Paramyotonia congenita without cold paralysis Paramyotonia congenita of von eulenberg Proximal myotonic dystrophy Ricker syndrome Ricker disease Von eulenberg disease Von eulenberg's disease Myotonic dystrophy 2 Myotonic dystrophy 2; dm2 Myotonic dystrophy caused by mutation in cnbp Myotonic syndrome |
Associated Genes (1) NCBI-RefSeq: CNBP (CCHC-type zinc finger nucleic acid binding protein) External Links: gnomAD browser Ensembl GeneCards
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| Cross-references of Myotonic dystrophy type 2 | OMIM | GARD | Orphanet | NCBI-GTR | NCBI-MedGen | MalaCards | MeSH | Annotations | |