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 nerve disorder causing uneven muscle weakness without significant numbness.
is dengue virus infection without noticeable symptoms, detected by testing.
is a rare, aggressive bone cancer causing multiple tumors over time.
is a mitochondrial disorder causing balance problems and nerve damage.
is a rare genetic disease causing coordination loss, telangiectasias, immune deficiency, cancer.
is a neurological disorder causing coordination problems (ataxia) and dementia.
is a genetic childhood-onset disorder causing ataxia and eye-movement difficulty.
is an inherited neurological disorder causing progressive ataxia and eye movement problems.
is a rare inherited disorder causing progressive ataxia from vitamin E deficiency.
is a rare genetic disorder causing ataxia, hearing loss, intellectual disability.
is a rare genetic condition with ataxia, hypogonadism, and vision loss.
is a genetic disorder causing ataxia, intellectual disability, eye-movement problems, cerebellar cysts.
is a rare inherited neurologic disorder causing coordination and eye-movement problems.
is a rare autosomal recessive disorder causing progressive ataxia and oculomotor apraxia.
is a rare genetic disorder causing movement unsteadiness and low blood counts.
is a genetic disorder causing coordination problems, light sensitivity, and short stature.
is a rare genetic disorder causing movement coordination problems and vision loss.
is a rare genetic disorder causing progressive ataxia and immune weakness.
is a milder genetic condition causing coordination issues and higher cancer risk.
is a rare inherited DNA-repair disorder causing progressive balance and coordination problems.
affects balance and coordination from early cerebellar injury, with variable severity.
is a rare, severe brain malformation where the forebrain fails to form.
is a rare genetic skeletal disorder causing severe bone and cartilage abnormalities.
is a rare, severe genetic bone disorder, often fatal around birth.