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 lifelong disorder causing coordination problems and intellectual disability.
is a type of interstitial lung disease causing inflammation and scarring.
is a birth condition causing missing skin, usually on the scalp.
is an inherited condition affecting nail growth, shape, or strength.
is an inherited condition causing abnormal nails without other health problems.
is an inherited condition causing abnormal fingernail and toenail development.
is an inherited condition affecting nail development without other body changes.
is a rare genetic condition affecting nail growth without other body changes.
is an inherited condition affecting nails without causing other body changes.
is a rare inherited condition causing abnormal or missing nails from birth.
is a genetic condition causing isolated nail abnormalities present from birth.
is an inherited condition causing abnormal nails from birth without other features.
is hearing loss without other symptoms, often inherited, severity and onset vary.
is thyroid enlargement without overactive hormone production, often causing neck swelling.
is a genetic disorder causing characteristic features, heart defects, and short stature.
is a genetic condition affecting growth, heart development, facial features, and learning.
is a genetic condition that can affect growth, heart, and development.
is a genetic condition that affects growth, development, and the heart.
is a genetic condition that affects growth, facial features, and the heart.
is a genetic condition affecting development, growth, and sometimes the heart.
is a genetic condition that affects development, growth, and heart health.
is a genetic condition that affects growth, development, and heart health.
is a genetic syndrome causing heart defects, short stature, and learning differences.
is a genetic condition affecting growth, facial features, heart, and development.