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 disorder causing gradual shrinking of tissues on one side.
is a rare disorder affecting brain white matter and ovarian function.
is a rare disorder with progressive microcephaly, seizures, cortical blindness, developmental delay.
is a rare, serious brain infection caused by JC virus.
is a rare motor neuron disease causing gradually worsening muscle weakness.
is a group of inherited disorders that cause worsening muscle weakness.
is a genetic epilepsy causing worsening seizures and muscle jerks (myoclonus).
is a rare inherited disorder causing seizures and sudden muscle jerks.
is a rare genetic epilepsy with progressive myoclonus (sudden jerks) and seizures.
is a rare genetic epilepsy causing worsening myoclonus, seizures, and coordination problems.
is a rare inherited epilepsy causing seizures, muscle jerks, and worsening coordination.
is a rare genetic epilepsy causing seizures, myoclonus, and progressive neurologic decline.
is a rare inherited epilepsy causing myoclonic seizures and progressive neurologic decline.
is a rare inherited epilepsy causing worsening seizures and muscle jerks (myoclonus).
is a rare disorder causing seizures, muscle jerks, and dystonia.
is a rare inherited disorder causing worsening seizures and nervous system decline.
is a rare group of disorders causing seizures, muscle jerks, and decline.
is a rare inherited disorder causing seizures, muscle jerks, and decline.
is a rare disorder causing steadily increasing skin and mucosal nodules.
is a condition causing gradually worsening speech and language difficulties.
is a rare spine condition causing gradual fusion of front vertebrae.
is a rare genetic disorder causing progressive bone formation in soft tissues.
is a fleshy eye growth that can slowly spread over the cornea.