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 condition affecting facial sensation and chewing, often causing pain.
is a rare tumor affecting the trigeminal nerve, causing facial symptoms.
causes sudden, severe facial nerve pain, often triggered by everyday touch.
is bladder irritation causing pelvic pain and frequent, urgent urination.
is a genetic syndrome causing triangular forehead, split nose, and acral anomalies.
is a rare genetic condition affecting skull shape, thumbs, growth, and development.
is a rare genetic condition causing triangular forehead, short stature, and delays.
is a rare childhood cancer with eye tumors and a brain tumor.
is a rare genetic condition causing inflammation in the digestive tract.
is a genetic muscle disorder causing progressive hip and shoulder weakness.
is an asthma caused by allergic reactions to trimellitic anhydride exposure.
is an allergic reaction to the antibiotic trimethoprim.
is a rare inherited disorder affecting energy production, muscles, blood, and brain.
is a rare inherited disorder affecting energy production, muscles, nerves, and blood.
is a rare genetic condition affecting thumb and hand development.
is a rare inherited disorder affecting the adrenal glands, swallowing, and tears.
is a rare genetic disorder affecting the adrenal glands, esophagus, and tears.
is a breast cancer that lacks estrogen, progesterone, and HER2 receptors.
is a rare chromosomal condition with an extra complete set of chromosomes.
is a rare genetic disorder causing limited mouth opening and bent fingers.
is a rare genetic condition caused by extra material on chromosome 10.
is a rare genetic condition caused by extra material from chromosome 12.
is a rare genetic condition causing severe birth defects and developmental problems.
is a rare chromosomal condition causing developmental delays and possible birth differences.