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 scar tissue on the retina that can blur vision.
is age-related trouble focusing on nearby objects, especially during reading.
causes localized loss of fat under the skin after repeated pressure.
are inherited disorders that impair nerve-to-muscle signaling and cause muscle weakness.
is when the water breaks before labor and before 37 weeks.
is a prolonged, often painful erection lasting more than four hours.
is a rare disorder where bone marrow stops making red blood cells.
is a condition where the adrenal glands do not make enough hormones.
is a rare growth that starts in the heart in adults.
is a rare, usually fatal brain infection caused by Naegleria fowleri.
is a rare skin condition causing soft, wrinkled patches from elastic loss.
is a rare inflammation of brain and spinal cord blood vessels.
is an eye disease causing sudden or gradual pressure-related vision loss.
is a rare immune disorder causing severe diarrhea and poor nutrient absorption.
is a rare inherited condition causing a small head and developmental differences.
is an inherited condition causing a very small head and developmental differences.
is a rare inherited condition causing a small head and developmental delays.
is an inherited condition causing a very small head and developmental delay.
is a rare inherited condition causing a small head and developmental delay.
is an inherited condition causing an unusually small head and developmental delay.
is a rare inherited condition causing a smaller head and developmental delays.