Condition: Lumbar hyperlordosis


rs864309488 in GMNN gene and Lumbar hyperlordosis PMID 26637980 2015 De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome.

rs878853220 in LMNA gene and Lumbar hyperlordosis PMID 27717888 2016 New intronic splicing mutation in the LMNA gene causing progressive cardiac conduction defects and variable myopathy.