rs2032582 is a genetic variant on gene ABCB1 associated with Inflammatory bowel disease 13.
rs10876864 is a genetic variant on gene IKZF4 associated with Intelligence and Allergic disease.
rs11540652 is a genetic variant on gene TP53 associated with Li-fraumeni syndrome 1 and Multiple myeloma.
rs104894226 is a genetic variant on gene HRAS associated with Costello syndrome and Large congenital melanocytic nevus.
rs7274581 is a genetic variant associated with Alzheimer's disease.
rs10808546 is a genetic variant associated with Abdominal aortic aneurysm.
is a rare inherited neuromuscular disorder causing fatigable muscle weakness from infancy.
is a genetic neuromuscular junction disorder causing fatigable muscle weakness from infancy.
is an inherited neuromuscular junction disorder causing fatigable muscle weakness, infancy-onset.
is a genetic neuromuscular junction disorder causing early, fluctuating muscle weakness.
is an inherited neuromuscular junction disorder causing early, fatigable muscle weakness.
causes inherited, early-onset, fluctuating muscle weakness from neuromuscular junction dysfunction.
is a rare inherited neuromuscular junction disorder causing fatigable muscle weakness.
is a genetic neuromuscular junction disorder causing early-onset fatigable muscle weakness.
is a genetic neuromuscular disorder causing early-onset muscle weakness and fatigability.
is an inherited nerve–muscle junction (neuromuscular) disorder causing fatigable muscle weakness.
is a genetic neuromuscular junction disorder causing early, fatigable muscle weakness.
is a genetic nerve-muscle signaling disorder causing early-onset muscle weakness, fatigability.
is a rare inherited neuromuscular disorder causing early-onset muscle weakness and fatigability.
is a genetic neuromuscular disorder causing early-onset fatigable muscle weakness and ptosis.
is a rare genetic neuromuscular disorder with fatigable muscle weakness.
is a rare inherited disorder causing early muscle weakness and breathing problems.
is a genetic nerve–muscle signal disorder causing early-onset weakness and fatigue.
is a genetic nerve-muscle disorder causing fatigable muscle weakness from birth.
is an inherited disorder causing early-onset muscle weakness and fatigability.
causes inherited neuromuscular junction weakness with fatigability, often starting in childhood.
are inherited neuromuscular disorders from glycosylation defects causing early-onset fatigable weakness.
is a group of inherited muscle disorders causing lifelong weakness from birth.
