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 inflammatory syndrome caused by acquired UBA1 gene mutations.
is a rare condition causing itchy hives after vibration or repetitive movement.
is a rare genetic disorder causing multisystem problems and severe developmental delays.
is a rare, usually low-grade cancer of the uterus lining.
is a rare cervical cancer subtype that usually grows slowly.
is a rare joint lining growth that causes pain, swelling, and stiffness.
is a gland cancer that forms fingerlike growths, often in the colon.
is a usually benign colon polyp that can sometimes become cancer.
is a rare tumor that causes severe watery diarrhea and low potassium.
is brain inflammation caused by a viral infection, often needing urgent care.
is an infection of the esophagus caused by certain viruses.
is a common viral rash illness that often causes fever.
is a viral stomach infection causing nausea, vomiting, diarrhea, and stomach cramps.
is a serious viral illness that can cause bleeding and organ damage.
is a liver infection caused by several different viruses.
is a condition.This condition is also known as Viral disease and Viral Infection.
is an inner ear infection causing sudden vertigo, nausea, and balance problems.
is a viral infection that inflames the voice box and causes hoarseness.
is an infection causing inflammation around the brain and spinal cord.
is a virus-related muscle inflammation causing pain, tenderness, and weakness.
is a lung infection caused by viruses that inflames air sacs.
is a rare viral skin condition causing tiny spines in immunosuppressed people.
is a rare, serious condition causing blood vessel calcification and organ damage.
involves birth defects of the liver, bile ducts, pancreas, or spleen.