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 tapeworm infection that usually affects sheep, goats, and cattle.
is a rare inherited hair disorder causing fragile, beaded hair.
is a rare genetic disorder affecting neurotransmitter breakdown, causing neurologic symptoms.
is a blood condition with abnormal antibody protein, usually harmless but monitored.
is a rare mast cell disorder causing repeated allergy-like symptoms.
is a condition with abnormal antibody proteins in the blood.
is an outward turning of one eye that may come and go.
is a rare immune disorder causing severe infections and blood problems.
is a cancer of monocyte-forming blood cells in the bone marrow.
is a disorder of low monocytes, causing recurrent or severe infections.
is a rare teratoma made mostly of one type of tissue.
is an eye condition with small misalignment and limited depth perception.
is a condition caused by a change in a single gene.
is an inherited disorder causing seizures and sometimes other health problems.
is a rare nerve condition causing weakness and wasting in one limb.
is a rare genetic condition that can affect development and body systems.
is a nerve disorder causing damage in multiple separate nerves.
is nerve damage in the leg causing pain, weakness, or numbness.
is nerve damage in the arm causing pain, weakness, or numbness.
is nerve damage in one or several arm nerves, causing pain.
is a rare soft tissue cancer that usually grows near joints.
is a rare genetic condition caused by missing chromosome 13 material.
is a chromosome 13 deletion that can cause developmental and health problems.
is a rare chromosome disorder affecting development and causing varied health problems.