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 cancer that starts in the skin's oil glands.
is a usually harmless skin gland tumor linked to Muir-Torre syndrome.
is a rare breast cancer that starts in oil-producing skin glands.
is a rare, aggressive skin cancer that often starts near the eye.
is a rare skin condition affecting the oil-producing glands.
is a skin condition affecting oil glands, causing bumps, irritation, or infection.
is a growth in oil glands that may be benign or cancerous.
is a rare skin condition causing many small, benign oil-gland cysts.
is a skin condition causing scaly inflamed patches that resemble psoriasis.
is a common skin condition causing dandruff, redness, and flaky patches.
is a common baby skin condition causing flaky, greasy, yellowish patches.
is a common, harmless skin growth that often appears with age.
is a rare genetic condition causing growth delay and a small head.
is a rare genetic condition with growth restriction and small head (microcephaly).
is a rare genetic condition causing growth delay and developmental differences.
is a rare inherited disorder causing severe growth delay and microcephaly.
is a rare inherited condition causing growth delay and developmental differences.
is a genetic condition causing growth delay, small head size, and delays.
is a rare inherited condition causing severe growth delay and microcephaly.
is a rare genetic disorder causing severe growth delay and microcephaly.
is a rare genetic disorder marked by poor growth and microcephaly.
is a rare inherited disorder causing growth delay and small head size.
is a birth defect causing a neck cyst, sinus, or opening.
causes some heartbeats to be delayed or blocked between chambers.