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 abnormally elevated, weakened diaphragm that can affect breathing.
is a rare genetic condition causing diaphragmatic hernia, short bowel, and asplenia.
is a birth defect affecting the diaphragm or abdominal wall.
is a rare inherited disorder causing long-bone marrow narrowing and sarcomas.
is frequent, loose, watery bowel movements that can cause dehydration.
is heart failure where the heart becomes stiff and fills poorly.
is a rare genetic bone disorder causing short stature and joint problems.
is a rare disorder causing dangerously low blood sugar from excess insulin.
causes episodes of low blood sugar from overactive insulin release.
causes low blood sugar when part of the pancreas makes excess insulin.
causes persistent low blood sugar from excess insulin in part of pancreas.
causes persistent low blood sugar from excess insulin despite diazoxide treatment.
causes repeated low blood sugar from excess insulin that responds to diazoxide.
is a serious clotting disorder that can cause dangerous bleeding.
is a rare inherited defect of dicarboxylic amino acid transport.
is an inherited condition that raises the risk of certain tumors.
is an allergic reaction to the pain reliever diclofenac.
is a liver fluke infection that usually affects the bile ducts.
is a rare condition where a person has two uteruses.
is a rare birth condition causing missing skin and oily birthmarks.
is a rare brain tumor affecting deep brain structures and body functions.
is a central brain tumor that may affect hormones and vision.
is a rare condition causing poor growth despite normal or increased appetite.
is a rare brain development disorder affecting the midbrain and nearby structures.