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 an allergic reaction to cefotaxime, ranging from rash to anaphylaxis.
is an allergic response to the antibiotic cefotiam, sometimes severe.
is an immune reaction to ceftazidime, ranging from rash to anaphylaxis.
is an immune reaction to the antibiotic ceftriaxone causing hives or anaphylaxis.
is an allergic reaction to cefuroxime, causing hives or anaphylaxis.
is an immune reaction to celery, sometimes causing life-threatening anaphylaxis.
is rare median arcuate ligament compression causing post-meal upper abdominal pain.
is an autoimmune condition triggered by gluten, damaging the small intestine.
is a rare genetic disorder combining celiac disease, seizures, and brain calcifications.
is a slow-growing, noncancerous tumor from a specific cell type.
is a malignancy starting in specific cells, potentially affecting many organs.
is a rare newborn kidney tumor, usually treated successfully with surgery.
is a benign, highly cellular uterine fibroid (leiomyoma) causing bleeding and pressure.
is a rare soft tissue cancer of fat, usually in limbs.
is a noncancerous nerve tumor with extra cells and dense fibers.
is an early-phase blood cancer with abnormal marrow growth and scarring.
is a usually benign nerve sheath tumor (schwannoma) that grows slowly.
is a bacterial skin infection causing redness, swelling, pain, and warmth.
is a rare genetic lymphatic condition causing chronic limb swelling in adulthood.
is a rare genetic disorder causing fused digits and limb abnormalities.
is an inherited eye disorder causing progressive central vision loss in adulthood.
is a benign milk duct growth causing nipple discharge or palpable lump.
is a rare corneal condition with central cloudy patches, usually asymptomatic.
is a rare disorder of central lymph vessels causing leakage and swelling.