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 genetic disorder causing weak immunity and facial, eye, skeletal differences.
is a rare inherited immune disorder causing recurrent infections and granulomas.
is a rare inherited condition causing infections, chronic diarrhea, and malabsorption.
is a rare inherited metabolic disorder causing acid buildup and energy problems.
is a rare inherited mitochondrial disease that impairs cellular energy production.
is a rare inherited mitochondrial disorder disrupting cellular energy production, often severe.
is an inherited mitochondrial disorder that affects energy production and development.
is an inherited mitochondrial disorder affecting energy production and multiple organs.
is a rare genetic mitochondrial disease affecting energy production and multiple organs.
is a rare mitochondrial disease causing low cellular energy and multi-system symptoms.
is a rare mitochondrial disorder affecting cellular energy production and multiple organs.
is a rare inherited mitochondrial disease affecting cellular energy production, often severe.
is a rare mitochondrial energy disorder causing multisystem symptoms and developmental delays.
is a rare inherited mitochondrial disorder reducing energy production, causing multisystem disease.
is a rare mitochondrial disorder affecting cellular energy production, causing multi-system symptoms.
is a rare genetic mitochondrial disorder disrupting energy production, affecting multiple organs.
is a rare mitochondrial disorder causing energy production failure and multisystem disease.
is a rare genetic mitochondrial disease causing early, multisystem energy-production problems.
is a rare genetic mitochondrial disorder causing energy failure and multi-organ symptoms.
is a rare inherited mitochondrial disease causing energy-production problems and multi-organ dysfunction.
is a rare inherited mitochondrial disorder that impairs cellular energy production.
is a rare inherited mitochondrial disorder affecting cellular energy production, often severe.
affects mitochondrial energy production, leading to weakness, developmental delays, organ problems.
is an inherited mitochondrial disease causing impaired energy production and multi-organ symptoms.