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 genetic connective tissue disorder causing joint hypermobility and fragile skin.
is a rare inherited disorder causing very loose joints and fragile skin.
is a rare inherited disorder causing very loose joints and stretchy skin.
is a rare inherited disorder causing fragile heart valves, skin, and joints.
is a genetic connective tissue disorder causing stretchy skin and hypermobile joints.
is an inherited connective tissue disorder causing stretchy skin and fragile joints.
is an inherited connective tissue disorder causing stretchy skin and joint looseness.
is a rare inherited connective tissue disorder affecting skin, joints, and healing.
is a rare inherited connective tissue disorder causing very fragile, sagging skin.
is a connective tissue disorder causing joint hypermobility, pain, and instability.
is a rare genetic disorder causing fragile tissues, weak muscles, and scoliosis.
is a rare inherited connective tissue disorder affecting joints, skin, and muscles.
is a rare inherited connective tissue disorder causing fragile tissues and contractures.
is a rare inherited connective tissue disorder causing short stature, loose joints.
is a rare inherited connective tissue disorder affecting bones, joints, and skin.
is a rare inherited disorder causing fragile bones and loose joints.
is a fast-growing experimental mouse tumor, not a standard human diagnosis.
is a tick-borne bacterial infection that can cause fever and flu-like symptoms.
is a rare genetic skeletal condition causing markedly delayed bone formation (ossification).
is a serious heart-lung complication caused by certain congenital heart defects.
is a rare skin condition causing loose, sagging patches of skin.
is a benign, slow-growing soft tissue growth beneath the shoulder blade.
is a rare connective tissue condition causing firm, elastic skin nodules.
is a rare skin condition causing small bumps in ring-shaped patterns.