GENE -- gene symbol (links to gene page)Condition -- named syndrome or disease+ -- predominantly adult-onset; pediatric cases documented
M56 entries · 18 genes, 38 conditions
Gene Symbols (18)
Conditions (38)
Malignant hyperthermiaMarinesco-Sjögren syndromeMcArdle disease (GSD V)Multicore/Minicore myopathyMyotubular myopathy (X-linked)MELASMERRFMIRASMöbius syndromeMohr-Tranebjaerg syndromeMorquio syndromeMulibrey nanismM\u00f6bius syndromeMacrophagic MyofasciitisMAGNESIUMMarinesco-Sj\u00f6gren syndromeMarkesbery (Late adult onset type IIb) Distal myopathyMöbius & Congenital facial syndromesMolecular Pathology: Immunohistochemistry for Inherited MyopathiesMonoclonal Gammopathies of Unknown Significance (& Other)Motor neuropathy-Motor neuron syndromesMultifocal Motor Neuropathy (MMN) & Immune Motor Neuropathies (IMN) 3,14Multisystem disordersMUSCLE BIOPSY STAINS & PROCEDURESMuscle Fiber PathologyMuscle Membrane ProteinsMUSCULOCUTANEOUS NERVEMyelin GlycoproteinsMyelin-Associated Glycoprotein (MAG; siglec-4) 1,4Myelin-related components, OtherMyofibrillar myopathies: GeneralMYOGLOBINURIA - RHABDOMYOLYSISMYOGLOBINURIA: Specific causesMyokymia & Benign Neonatal Epilepsy (BFNS1)Myopathic TremorMyopathies & NMJ Disorders: Antibodies & ComplementMyotonia Congenita, Dominant (Thomsen)Myotonic Dystrophy 1 (DM1)
Data sourced from the Washington University Neuromuscular Disease Center, NCBI Gene, and OMIM. For clinical use, always refer to primary sources.