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 benign orbital vascular tumor, often causing painless eye bulging.
is a usually benign, slow-growing meningeal tumor near the cavernous sinus.
is a rare, life-threatening clot in a vein behind the eyes.
is fly larvae infestation of body cavities, causing pain and tissue damage.
is a rare inherited glycosylation disorder causing multi-system symptoms from infancy.
is a genetic neurodevelopmental disorder causing severe intellectual disability and distinctive features.
is a rare inherited immune disorder causing severe T-cell deficiency and infections.
is a rare inherited immune disorder causing recurrent infections and poor growth.
is a rare inherited immune disorder impairing T-cell signaling, causing recurrent infections.
is an inherited immune disorder causing recurrent infections and low antibodies.
is a rare inherited primary immunodeficiency causing severe, recurrent infections.
is a rare genetic disorder causing heart defects, developmental delays, facial differences.
is a rare genetic disorder causing early seizures and severe developmental delays.
is a rare inherited disorder causing inflammation, infections, and neutrophil problems.
affects the first part of the large intestine, causing inflammation and pain.
is a colon cancer starting in the cecum, often symptomless early.
is a benign growth (polyp) in the cecum that can become cancerous.
is a colorectal cancer starting in the cecum, the large intestine.
is a type of colorectal cancer that begins in the cecum.
is a rare gut lymphoma starting in the cecum, often treatable.
is a rare inherited disorder affecting brain development, nerves, and skin.
is an immune reaction to cefaclor, causing rashes or anaphylaxis.
is an immune reaction to cefixime causing rash, hives, breathing trouble.