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ABCDEFGHIJKLMNOPQRSTUVWXYZA-Z Index
GENE -- gene symbol (links to gene page)Condition -- named syndrome or disease+ -- predominantly adult-onset; pediatric cases documented
L26 entries · 14 genes, 12 conditions
Gene Symbols (14)
L1CAML2HGDHLARGE1LDHALDB3 (ZASP)†LITAF+LMOD3LONP1LRP4LRP12LRPPRCLRSAM1†LMNALRSAM1\U2020
Conditions (12)
Lafora disease+Laing distal myopathyLeber hereditary optic neuropathyLeigh syndromeLimb-girdle muscular dystrophy (LGMD)L5 RadiculopathyLEPROSYLipid Myopathies: Clinical classificationLipids: GeneralLong QT SyndromesLower Motor Neuron Syndrome: Proximal Arm Predominant 1,Lumbosacral Plexus

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