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 genetic condition causing fragile bones, blindness, and loose joints.
is a rare genetic condition with fragile bones and lighter coloring.
is a rare genetic disorder causing fragile bones and early vision loss.
is a jawbone complication after radiation therapy that damages bone tissue.
is an aggressive bone cancer starting in bone-forming cells, often adolescents.
is cancer that can develop in bones affected by Paget's disease.
is a condition where bones become abnormally dense and hard.
is a rare genetic disorder causing dense bones, developmental delay, and craniosynostosis.
is a very rare genetic syndrome affecting bones, skin, and ovarian function.
is a rare genetic bone disorder causing dense, abnormally shaped long bones.
is a rare plasma cell disorder causing hardened bones and whole-body symptoms.
is a stomach parasite infection that mainly affects cattle and causes diarrhea.
is an acquired skin condition that affects the skin in various ways.
is a skin condition affecting the dermis, with varied causes and symptoms.
is a group of skin conditions affecting the epidermis, causing varied symptoms.
is a rare inherited skin disorder caused by genetic changes.
is a group of inherited skin disorders affecting the epidermis.
is an immune disorder mainly affecting antibody production and infection defense.
are rare disorders where the body's first-line defenses do not work properly.
is a group of disorders that disrupt how the body uses energy.
is a group of inherited metabolic disorders that can cause seizures.
is a group of metabolic disorders that can affect the skin.
is a rare group of diabetes disorders with uncommon underlying causes.
is a rare genetic syndrome affecting brain development and other body systems.