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 congenital disorder where tight bands restrict limbs or digits.
is stiffening of the heart lining (pericardium) that restricts filling.
is eyelid and eye surface inflammation from irritants or allergies.
is a noncontagious, itchy skin rash from irritants or allergens.
is corneal swelling from contact lens wear, causing blurred vision and discomfort.
is a viral skin infection from sheep or goats causing painful pustules.
is a childhood epilepsy with sleep-activated EEG, seizures, and developmental regression.
is a genetic disorder causing contractures, developmental delay, and Pierre Robin sequence.
is a rare genetic disorder with contractures, ectodermal changes, and cleft lip/palate.
is a genetic condition with contractures, webbed neck, small jaw, underdeveloped nipples.
is rare genetic condition causing joint contractures, skin webbing, and spinal/wrist/ankle fusions.
is a tumor at the spinal cord's end, affecting legs and bladder.
is a benign fatty mass at the lower spinal cord, sometimes tethering.
is a rare, aggressive cancer of blood or lymph vessel linings.
is a rare soft-tissue cancer from fibroblasts, often in limbs or trunk.
is a rare smooth muscle cancer, usually in uterus, abdomen, limbs.
is a common benign fatty tumor under skin, soft and movable.
is a rare vascular soft tissue cancer that can metastasize (spread).
is a fast-growing bone cancer near the knee requiring chemotherapy and surgery.
is a functional neurological disorder causing symptoms without structural disease, often stress-related.
is a rare genetic condition affecting hand and foot development.
is a rare genetic condition causing developmental delays and distinctive features.
is spinal cord dysfunction from low copper, causing gait and sensation problems.
is right-heart failure from lung disease causing high lung artery pressure.