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 a genetic disorder causing nerve sheath tumors and often chronic pain.
is a rare chromosome condition causing variable birth defects and developmental delays.
is a rare chromosomal condition with extra chromosome 10 in some cells.
is a genetic condition with an extra chromosome 12 in some cells.
is a rare genetic condition causing varied growth, developmental, and body differences.
is a rare genetic condition caused by extra chromosome 15 cells.
is a condition where some cells carry extra chromosome 16, variable outcomes.
is a rare chromosomal condition causing varied growth, developmental, and health problems.
is a rare chromosome condition causing variable growth and developmental differences.
is a rare chromosomal condition that can affect growth, development, and health.
is a rare chromosomal condition causing variable growth, developmental, and physical differences.
is a rare chromosomal condition causing varied birth defects and developmental delays.
is a rare chromosome condition causing varied birth defects and developmental differences.
is a rare condition with extra chromosome 5 in some cells.
is a rare condition caused by extra chromosome 8 in some cells.
is a rare genetic condition with an extra chromosome 9.
is a genetic disorder causing abnormal chromosomes, growth problems, and cancer risk.
is a rare genetic disorder causing chromosomal instability (aneuploidy), developmental delays, cancers.
is a rare genetic disorder causing mosaic aneuploidy, growth restriction, developmental delays.
is a rare genetic disorder causing chromosome errors and developmental problems.
is diarrhea caused by food moving too quickly through the intestines.
is nausea, dizziness, and vomiting from conflicting motion signals to the brain.
affects the nerves controlling muscles, causing weakness and movement problems.