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.
causes severe early childhood vision loss from inherited retinal dysfunction.
is an inherited retinal disorder causing severe vision loss from birth.
is an inherited eye disorder causing severe vision loss from birth.
is a rare inherited eye disease causing severe vision loss in infancy.
is a rare inherited eye disorder causing severe vision loss from birth.
is a genetic eye disorder causing severe vision loss from infancy.
is a rare inherited eye disorder causing severe vision loss from infancy.
is an inherited retinal disorder causing severe vision loss from infancy.
is a rare genetic retinal disorder causing severe vision loss from infancy.
is an inherited retinal disorder causing severe vision loss in infancy.
is an inherited eye disorder causing severe vision loss from infancy.
is a rare inherited condition causing severe vision and early hearing loss.
is an inherited mitochondrial disease causing sudden, painless central vision loss.
is an inherited condition causing sudden vision loss and movement problems.
causes sudden vision loss and sometimes demyelinating disease in brain and spine.
is a rare inherited mitochondrial disorder affecting vision and the nervous system.
is a benign foot condition (plantar fibromatosis) causing arch nodules and pain.
is a parasitic infestation where leeches attach and feed on blood.
is a heart conduction problem affecting the electrical signal's path.
is a rare birth condition with complex heart and organ arrangement differences.
is a rare heart condition where the left ventricle develops abnormally.
is a broad term for skin conditions affecting the legs.
is a childhood hip disorder caused by reduced blood flow to the thighbone.
is a bacterial infection that can cause severe pneumonia and flu-like illness.