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 mitochondrial disease causing impaired cellular energy and multi-system problems.
is a rare inherited mitochondrial disorder causing multi-system energy failure.
is a rare inherited mitochondrial disorder affecting energy production across systems.
is a rare inherited enzyme disorder causing fat malabsorption and poor growth.
are inherited disorders causing multiple pituitary hormone deficiencies (hypopituitarism).
is a lung condition with scarring and airspace damage causing breathlessness.
is a rare genetic immune disorder causing severe, recurrent infections in infancy.
is a rare thymus gland tumor combining different thymoma subtypes.
is a high-grade, noninvasive ductal breast cancer with central dead cells (necrosis).
is an infection caused by normally harmless body bacteria after disruption.
is a congenital pit at mouth corner; usually harmless, may drain saliva.
is a disorder affecting bile flow from liver to small intestine.
is a growth in the bile duct that may be cancerous.
is a mild viral upper respiratory infection (URI) causing congestion, runny nose.
is a birth-present lymphatic vessel malformation causing soft, fluid-filled cysts.
is nerve injury, often compression, causing foot drop, numbness, and weakness.
is an immune system disorder with low antibodies, recurrent infections, autoimmunity.
is a primary immune disorder with low antibodies (immunoglobulins) and recurrent infections.
is an immune disorder with low antibodies, causing recurrent infections.
is a primary immunodeficiency with low antibodies and recurrent infections.
is a genetic immune disorder causing low antibodies and recurrent infections.
is a primary immune disorder causing low antibodies and recurrent infections.
is a genetic immune disorder causing low antibodies, recurrent infections, and autoimmunity.