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 neurodevelopmental disorder causing hypotonia, repetitive hand movements, and impaired language.
is a neurodevelopmental disorder with involuntary movements and developmental differences.
is a neurodevelopmental disorder that often causes language delay and seizures.
affects brain development, with small head (microcephaly), cataracts, and kidney problems.
is a neurodevelopmental disorder involving midbrain and hindbrain malformations.
is a neurodevelopmental disorder causing movement, speech, eye, and brain problems.
is a rare disorder causing poor growth, spasticity, and hearing loss.
is a neurodevelopmental disorder causing regression, abnormal movements, speech loss, and seizures.
is a neurodevelopmental disorder with short stature, prominent forehead, and feeding difficulties.
is a rare genetic condition causing developmental delays, spasticity, and poor growth.
is a neurodevelopmental disorder causing speech problems and distinctive facial features.
is a rare genetic condition affecting development, facial features, heart, and bones.
is a rare genetic disorder affecting skin, hair, and the nervous system.
is a rare tumor arising from nerve-related embryonic tissue.
is a rare cancer that starts in hormone-making nerve cells.
is a rare pancreatic cancer that starts in hormone-making cells.
is a rare childhood lung disease causing fast, difficult breathing.
is a rare tumor that starts in hormone-making neuroendocrine cells.
is a usually slow-growing tumor that starts in the appendix.
is a rare esophageal cancer arising from hormone-producing neuroendocrine cells.
is a rare pancreatic tumor that makes hormones or grows silently.