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 birth defect affecting the windpipe and sometimes breathing.
is calcium buildup in the windpipe, often harmless and age-related.
is a rare cancer that starts in the windpipe (trachea).
is a condition affecting the windpipe, causing breathing or coughing problems.
is a rare cancer affecting lymph tissue in the windpipe (trachea).
is a narrowing of the windpipe that can make breathing difficult.
is an infection and inflammation of the windpipe that can affect breathing.
is a rare airway disorder causing bony nodules in the windpipe.
is an eye infection that can lead to blindness without treatment.
is a rare genetic condition affecting the heart, development, and facial features.
is a rare inherited metabolic disorder that can affect multiple organs.
is a rare inherited disorder impairing vitamin B12 (cobalamin) transport, causing deficiency.
is a rare inherited condition causing low blood B12, usually asymptomatic.
is a rare inherited disorder causing vitamin B12 transport problems.
causes worsening thickened skin on the palms and soles over time.
is a temporary joint inflammation that usually gets better on its own.
is temporary joint pain and stiffness that usually improves on its own.
is a brief loss of blood flow to the brain.
is a temporary thyroid hormone deficiency present at birth.
is a temporary thyroid hormone problem in newborns caused by maternal factors.
is a temporary low-thyroid condition in newborns caused by neonatal factors.
is a temporary childhood anemia caused by reduced red blood cell production.
causes short-lived newborn jaundice (hyperbilirubinemia) due to inherited processing differences.
is a sudden, temporary episode of memory loss without other neurological symptoms.