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 delayed stomach emptying without a known cause, causing nausea and fullness.
is a seizure disorder causing generalized seizures, often genetic, medication-responsive.
is a genetic epilepsy syndrome causing generalized seizures, often beginning in childhood.
is a seizure disorder causing recurrent generalized seizures without a known cause.
is a genetic epilepsy causing recurrent seizures that affect both brain sides.
is an inherited epilepsy syndrome causing generalized seizures, often beginning in childhood.
is an inherited epilepsy syndrome causing generalized seizures, often starting in childhood.
is an inherited epilepsy causing recurrent generalized seizures, often beginning in childhood.
is an inherited seizure disorder causing generalized seizures, often beginning in childhood.
is a genetic epilepsy causing recurrent generalized seizures, often starting in childhood.
is a rare inherited epilepsy causing generalized seizures, often starting in childhood.
is a genetic epilepsy causing repeated seizures from widespread brain activity.
is an inherited epilepsy syndrome causing recurrent generalized seizures.
is a rare, severe heart inflammation that can rapidly cause heart failure.
is a rare childhood seizure disorder causing weakness on one side.
is excess calcium in the urine without a clear cause.
is persistent eosinophilia (high eosinophils) without known cause, damaging multiple organs.
is a sleep disorder causing excessive daytime sleepiness despite enough sleep.
is a group of autoimmune muscle diseases causing weakness and inflammation.
is a group of lung diseases causing inflammation and scarring.
causes increased pressure around the brain without a known cause.
is a smaller-than-expected penis without other known health or genetic conditions.