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 nerve disorder causing progressive leg stiffness and weakness.
is a rare inherited disorder causing progressive leg stiffness and weakness.
is a rare inherited nerve disorder causing leg stiffness (spasticity) and weakness.
is an autosomal recessive nerve disorder causing leg stiffness (spasticity) and weakness.
is a rare genetic nerve disorder causing progressive leg stiffness and weakness.
is a rare autosomal recessive disorder causing progressive leg stiffness and weakness.
causes progressive leg stiffness (spasticity) and weakness; autosomal recessive, rare.
is a rare inherited condition causing leg spasticity, weakness, and walking problems.
is a rare inherited disorder causing progressive balance and coordination problems.
is a rare inherited disorder causing progressive balance and coordination problems (ataxia).
is a rare inherited disorder causing progressive coordination, balance, and speech problems.
is a rare inherited childhood-onset cerebellar disease causing progressive coordination loss.
is a rare inherited disorder causing progressive loss of coordination (ataxia).
