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 eye disorder causing corneal swelling, iris changes, and glaucoma.
is a genetic ion channel disorder causing recurrent seizures and neurological symptoms.
is a rare fat-based spinal growth tethering the conus medullaris.
is a rare viral hemorrhagic fever causing high fever, bleeding, organ damage.
is a rare genetic condition affecting the heart, face, and fingers.
is an inherited peripheral nerve disorder causing progressive muscle weakness and numbness.
is a hereditary nerve disease (neuropathy) causing progressive weakness and numbness.
is a hereditary nerve disorder causing progressive weakness, numbness, and foot deformities.
is a genetic nerve disorder causing progressive weakness and numbness in limbs.
is an inherited peripheral nerve disease causing weakness, numbness, and foot problems.
is an inherited peripheral nerve disorder causing progressive weakness and numbness.
is an inherited nerve disorder causing muscle weakness, numbness, and foot problems.
is an inherited nerve disorder causing slowly progressive weakness and numbness.
is a hereditary neuropathy causing progressive distal weakness and sensory loss.
is an inherited peripheral nerve disorder causing progressive limb weakness and numbness.
is a hereditary axonal neuropathy causing progressive distal weakness and sensory loss.
is an inherited peripheral neuropathy causing progressive distal weakness and sensory loss.
is an inherited nerve disorder causing progressive limb weakness and sensation loss.
is a hereditary nerve disorder causing progressive limb weakness and sensory loss.
is a genetic peripheral neuropathy causing progressive weakness and sensory loss.
is hereditary nerve damage (neuropathy) causing progressive limb weakness and numbness.
is a genetic peripheral nerve disorder causing progressive weakness and numbness.