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 genetic disorder causing poor growth, developmental delays, and abnormalities.
involves corneal surface layer damage causing pain, light sensitivity, and blur.
is damage to the arm's nerve network causing weakness, numbness, pain.
is a benign or malignant tumor of the shoulder and arm nerves.
is inflammation of shoulder nerves causing sudden pain, weakness, and numbness.
is nerve damage affecting shoulder-to-hand function, causing pain, weakness, numbness.
is a rare genetic condition causing flat head, long eyelashes, developmental delay.
is a rare skeletal condition causing short stature and shortened fingers/toes (brachydactyly).
is a congenital genetic condition causing unusually short fingers and toes.
is a hereditary condition causing shortened fingers from absent middle bones.
is a hereditary hand and foot condition with shortened fingers and toes.
is an inherited hand and foot condition causing shortened middle bones.
is a genetic condition causing short fingers and toes from bone underdevelopment.
is an inherited difference with short digits (brachydactyly), mainly the index.
causes short little fingers from shortened middle phalanx, usually inherited.
is a genetic condition causing shortened fingers and toes, usually mild.
is a rare genetic condition causing shortened fingers and toes, variably severe.
is a rare inherited condition causing shortened bones in hands and feet.
is a genetic condition causing short or missing finger and toe bones.
is an inherited condition causing shortened or missing finger and toe tips.
is a rare inherited condition causing shortened fingers/toes and nail underdevelopment.
is a congenital hand condition causing shortened finger bones, often autosomal dominant.
is an inherited short thumb tip with small nail, usually harmless.
is a genetic condition causing variably shortened hand and foot bones.