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 appendix cancer that can spread within the abdomen.
involves appendix inflammation or disorders causing right-lower abdominal pain.
is a rare, benign smooth muscle tumor of the appendix, often incidental.
is a rare cancer of appendix lymph tissue, often mimicking appendicitis.
is a rare appendix cancer producing mucus, sometimes causing pseudomyxoma peritonei.
is a visual processing disorder causing difficulty recognizing objects despite sight.
is an allergic reaction to apples, causing mouth itching and hives.
is a brain-based movement planning disorder causing difficulty performing learned actions.
is an immune reaction to apricots causing itching, hives, or anaphylaxis.
is a rare, severe brain malformation with absent forebrain structures, often fatal.
is a severe, rare birth defect of the forebrain and cerebellum.
is a rare, severe congenital brain malformation affecting forebrain development, often fatal.
causes rapid wrinkling and swelling of palms and soles after water exposure.
is a rare eye emergency with shallow chamber and elevated pressure.
is a genetic disorder with long fingers (arachnodactyly), abnormal bones, intellectual disability.
is a rare genetic condition causing arachnodactyly (long fingers), intellectual disability, dysmorphism.
is a fluid-filled sac in the brain or spinal cord.
is inflammation of the spinal arachnoid membrane causing chronic nerve pain.
is a viral illness spread by mosquitoes or ticks, causing fever.
is a gray-white corneal ring from cholesterol deposits, usually harmless.
is a rare genetic condition affecting development across multiple body systems.
is anemia from low red blood cell production, causing fatigue and pallor.
is a viral infection usually spread by rodents, causing fever and malaise.
is a Junín virus disease from rodents in Argentina causing bleeding.