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 chronic inflammation of colon and rectum causing diarrhea and bleeding.
is a painful inflammatory mouth condition causing sores and eating discomfort.
is a bacterial infection causing a skin ulcer and swollen lymph nodes.
is a rare skin condition causing eyebrow redness, roughness, and thinning.
is a genetic muscle disorder causing weakness, stiff joints, and breathing problems.
is a rare genetic condition with ulna underdevelopment and intellectual disability.
is a rare genetic bone disorder affecting forearm growth and development.
is a rare birth difference where part of the ulna is missing.
is a rare genetic condition affecting forearm and foot development.
affects the nerve along the inner arm, causing numbness and weakness.
is nerve damage affecting the hand and forearm, causing numbness and weakness.
is a rare genetic disorder affecting limb development, glands, and puberty.
is a rare genetic condition causing underdeveloped arm and leg bones.
is a rare birth condition linking intestinal blockage with umbilical cord ulcers.
is a belly-button bulge from abdominal wall weakness, common in infants.
is an inherited kidney disorder causing scarring and progressive kidney failure.
is a fast-growing blood and bone marrow cancer without a specific subtype.
is a rare inflammatory condition causing repeated fevers and other symptoms.
is a rare childhood inflammatory disorder causing repeated fevers and other symptoms.
is a heart muscle disease that does not fit standard types.
is a genetic skin condition with features that can vary widely.
is a rare disorder causing blocked-bowel symptoms without a physical blockage.
is a bone marrow disorder causing abnormal blood cells.
is a rare blood cancer causing abnormal and excess blood cells.