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 genetic mitochondrial disease causing energy failure and multisystem symptoms.
is a rare mitochondrial disorder causing severe energy production problems in infancy.
is a rare inherited mitochondrial disorder reducing cellular energy, affecting multiple organs.
is an early-onset genetic mitochondrial disease impairing energy production across organs.
is a rare genetic mitochondrial disorder affecting energy production and multiple organs.
is a rare mitochondrial disorder causing multi-system energy failure and developmental problems.
is a rare mitochondrial disease causing energy-production failure and multi-organ symptoms.
is a rare inherited mitochondrial disease causing energy-production failure and multisystem illness.
is an inherited mitochondrial disorder causing early multisystem disease and lactic acidosis.
is a rare inherited mitochondrial disease causing energy failure and multisystem involvement.
is a rare genetic mitochondrial disorder disrupting energy production, causing multisystem symptoms.
is a rare genetic mitochondrial disease impairing cellular energy production, often severe.
is a rare genetic mitochondrial disorder causing severe, early-onset multisystem energy failure.
is a rare inherited mitochondrial disease impairing cellular energy production, often severe.
is a rare mitochondrial disorder causing multisystem energy failure and lactic acidosis.
is a rare genetic mitochondrial disorder causing multi-organ energy production problems.
is a rare inherited mitochondrial disorder affecting energy production (oxidative phosphorylation).
is a rare inherited mitochondrial disease causing multi-system energy production failure.
is a rare inherited mitochondrial disease causing early-onset, multi-system energy production failure.
is a rare inherited mitochondrial disorder impairing energy production, often multisystem.
