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 loss of body fat after birth, causing metabolic complications.
is a non-inherited metabolism disorder that disrupts energy use and balance.
happens after exposures that raise methemoglobin, reducing oxygen delivery and causing cyanosis.
is a kidney tubule disorder from monoclonal light chains, causing electrolyte wasting.
is a progressive disease affecting motor neurons, causing weakness and wasting.
is a disorder where nerve-muscle communication fails, causing weakness and fatigue.
is low neutrophils (white blood cells) after birth, increasing infection risk.
is reduced night vision (nyctalopia) developing later from treatable underlying causes.
is a rare condition causing gradual loss of upper-body subcutaneous fat.
is a movement disorder caused by peripheral nerve or muscle damage.
is nerve damage outside brain and spinal cord, causing numbness, tingling, weakness.
is a pituitary disorder developing after birth, causing low hormone levels.
is a noninherited rise in red blood cells, increasing clot risk.
is a condition where brain cavities form after injury, bleeding, or infection.
is acquired loss of ovarian function before 40, causing infertility, low estrogen.
is a bleeding disorder from reduced factor II (prothrombin) activity.
is a rare condition causing PXE-like skin changes from damaged elastic fibers.
is a sudden, life-threatening clotting disorder causing widespread skin bruising and necrosis.
is a brain disorder with acquired cerebral clefts causing seizures, weakness.
is increased red blood cells from low oxygen or excess erythropoietin (EPO).
is damage to sensory nerve clusters causing numbness, pain, and imbalance.
is a non-inherited muscle disease (myopathy) causing weakness and fatigue.
is narrowing of the tear duct (nasolacrimal duct), causing tearing and infections.
is a low platelet count acquired after birth, causing bleeding and bruising.