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 an eye condition causing gradual central vision changes from retinal cysts.
is a parasitic intestinal infection that usually causes watery diarrhea.
are abnormal pockets or passages affecting the mouth, jaw, or face.
is a rare genetic disorder affecting hormone production and development.
is a rare inherited mitochondrial disorder that impairs the body's energy production.
is a serious cytomegalovirus infection affecting people with weakened T-cell immunity.
is an eye infection from cytomegalovirus that can threaten vision.
is a rare inflammatory disease affecting fatty tissue under the skin.
is a rare inherited disorder causing bleeding due to platelet dysfunction.
is a very rare genetic syndrome that affects development and physical features.
is a rare genetic metabolic disorder that can affect brain development.
is a rare inherited metabolic disorder causing developmental delays, seizures, and hypotonia.
is a rare genetic disorder affecting brain development and body chemistry.
is a rare inherited disorder that causes harmful buildup of D-glyceric acid.
is a rare allergy to mannitol, a sweetener used in foods.
is a rare inherited disorder that affects brain development and movement.
is an infection of the tear sac causing pain and swelling.
is a rare genetic disorder causing tear duct inflammation and bone spots.
is a tear duct blockage causing a cyst-like swelling near birth.
is a rare genetic disorder affecting development, growth, and sometimes learning.
is a rare genetic condition affecting brain development and causing extra digits.
is a rare brain development condition affecting balance, movement, and sometimes learning.
is a rare inherited disorder affecting the heart, muscles, and sometimes learning.
is an inherited skin condition causing scaly bumps, nail changes, and flares.