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 progressive hair loss on the scalp.
is a rare inherited condition causing sparse hair and early vision loss.
is a rare genetic condition causing sparse hair and hearing loss.
is a rare genetic condition causing sparse hair and intellectual disability.
is a rare inherited disorder causing sparse hair, limb swelling, and telangiectasias.
is a genetic disorder causing sparse hair, swelling, telangiectasias, and kidney problems.
is a rare genetic disorder affecting hair, bones, gums, and skin.
is an eye misalignment where one eye turns downward.
causes excess uric acid and can sometimes affect movement and behavior.
is a rare inherited disorder affecting purine recycling and the nervous system.
is a rare toxin-related illness caused by too much botulinum treatment.
is a rare prion disease caused by contaminated medical treatment or equipment.
is a genetic disorder causing immune problems, developmental delays, and distinctive features.
is a group of skin conditions causing very dry, thick, scaly skin.
is a rare genetic disorder causing scaly skin, hair loss, and photophobia.
is a rare genetic skin disorder causing thick, spiky, scaly skin.
is a common inherited skin disorder causing dry, scaly skin.
is a rare genetic syndrome affecting skin, hair, eyelids, lips, and development.
is a rare inherited disorder affecting skin, liver, spleen, and coordination.
is a rare inherited disorder causing dry, scaly skin and sparse hair.
is a rare inherited disorder affecting skin, learning, growth, and kidneys.
is a rare genetic disorder causing scaly skin, mouth, and finger changes.
is a rare inherited disorder causing premature birth and scaly skin.
is a rare genetic disorder affecting skin, growth, fingers, and eye lenses.