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 skin lymphoma involving aggressive γδ T cells.
is a rare skin lymphoma caused by abnormal gamma/delta T cells.
is a rare cancer that starts in immune cells in the skin.
is a slow-growing skin lymphoma involving B cells and usually excellent outcomes.
is a rare skin lymphoma caused by abnormal mature T cells.
is a rare skin disorder causing reddish-brown patches from plasma cell buildup.
is a rare skin lymphoma causing patches, plaques, tumors, or itching.
is a rare skin lymphoma caused by cancerous T cells.
is a rare skin infection caused by tuberculosis bacteria.
is a rare scalp condition causing thick folds and deep grooves.
is a rare colon disorder causing severe constipation and slow bowel movement.
is a fast-growing brain or spinal cord lymphoma that starts there.
is a rare inherited movement disorder causing involuntary twisting and abnormal postures.
is a rare inherited movement disorder causing involuntary muscle contractions and twisting.
is an inherited movement disorder causing involuntary muscle contractions and abnormal postures.
is a movement disorder causing involuntary muscle contractions and abnormal postures.
is an inherited eye disease that raises pressure and can damage vision.
is a rare, aggressive lymphoma causing fluid buildup around organs.
is a rare disorder where eosinophils inflame the digestive tract.
is a rare disorder with burning pain, redness, warmth in extremities.
is a rare, harmless condition causing thick folds on the scalp.