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 rare inherited condition causing short stature and low antibody levels.
is a rare genetic condition causing short stature from impaired growth signaling.
is a rare genetic disorder affecting growth hormone-IGF system, causing short stature.
is a condition causing short stature, advanced bone age, and early osteoarthritis.
is a rare genetic syndrome affecting growth, hearing, the jaw, and bones.
is a genetic disorder causing short stature, short digits, obesity, developmental delays.
is a rare genetic condition affecting growth, facial development, and genital formation.
is a rare genetic syndrome causing short stature, deafness, and immune problems.
is a rare inherited disorder causing slow growth and delayed bone development.
is a rare genetic condition affecting growth, nails, hair, and facial features.
is a genetic disorder causing short stature, optic atrophy, and blood changes.
is a rare condition causing short stature and pituitary-brain abnormalities.
is a rare genetic syndrome affecting growth, vision, hearing, and development.
is a rare genetic condition causing short stature and heart valve disease.
is a genetic condition causing short stature, webbed neck, and heart problems.
is a rare genetic disorder causing short stature and heart malposition.
is a rare genetic condition causing short height and skeletal differences.
is a genetic condition causing short stature, facial-skeletal differences, sometimes heart differences.
is a rare genetic condition with short stature and insulin resistance.
is a rare genetic condition affecting the feet, eyelashes, and development.
is a rare genetic condition causing short forearms, hypotonia, and intellectual disability.
is a rare genetic disorder causing short limbs and severe immune deficiency.
is a rare cilia-related bone disorder causing small chest and polydactyly.
is a rare genetic skeletal disorder causing narrow chest and short limbs.