GENE -- gene symbol (links to gene page)Condition -- named syndrome or disease+ -- predominantly adult-onset; pediatric cases documented
I23 entries · 7 genes, 16 conditions
Gene Symbols (7)
Conditions (16)
I. Clinical Indications for Measurement of anti-MAG antibodiesII. Results with Specificity and Sensitivity for Sensory-Motor NeuropathiesIII. Testing Laboratory Standards for anti-MAG Antibodies.Immune & Inflammatory Myopathies: Neoplasm AssociationsIMPP (Myofasciitis; EVIM) + Deafness: Enterovirus & Hypogammaglobulinemia-RelatedInclusion Body Myopathy with Paget disease of Bone & Dementia 1 (IBMPFD1)Inclusion Body Myositis (IBM)Inflammatory & Immune Myopathies (IIM): AcquiredInflammatory Myopathy + Mitochondrial Pathology in muscle (IM-Mito), subtype of IM-VAMPInflammatory Myopathy with Abundant Macrophages (IMAM)ION CHANNELS, TRANSMITTERS, RECEPTORS & DISEASEIsaac's SyndromeItch: Anatomy & PhysiologyItch: Clinical SyndromesIV. Interpretations of Confirmed Positive anti-MAG ResultsIV. Positive Result: Clinical Utility and Interpretations
Data sourced from the Washington University Neuromuscular Disease Center, NCBI Gene, and OMIM. For clinical use, always refer to primary sources.