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 genetic condition causing developmental, speech, learning, and behavioral differences.
is a rare genetic condition causing developmental delays and speech-language difficulties.
is a rare chromosome 8p rearrangement causing developmental delay and congenital anomalies.
is a rare chromosomal microdeletion causing developmental delays, learning difficulties, and anomalies.
is a chromosomal duplication causing variable developmental, learning, and heart differences.
is a genetic deletion causing developmental delays, heart defects, and learning differences.
is a rare genetic condition from extra 8q12 DNA, with variable symptoms.
is a rare chromosome 8 deletion causing developmental, learning, and health problems.
is a rare chromosome deletion causing developmental delay, intellectual disability, congenital anomalies.
is a rare chromosome deletion causing developmental delays and speech impairment.
causes developmental delays, speech and learning difficulties, distinctive features, congenital anomalies.
is a rare chromosome deletion causing developmental delay, speech impairment, and seizures.
is a rare chromosome 9 deletion causing developmental delays and variable features.
is a rare chromosome deletion causing developmental delays, intellectual disability, seizures.
is a fast-growing cancer of B lymphocytes, often curable with chemoimmunotherapy.
is amyloid A protein buildup damaging organs, often kidneys, from chronic inflammation.
is a rare inherited amyloidosis causing organ protein deposits and dysfunction.
is a rare inherited disorder causing amyloid buildup in organs.
is a rare inherited amyloidosis causing protein deposits in organs.
is a rare X-linked genetic condition affecting face, growth, and genitals.
is a rare congenital condition with hypoplastic anemia and limb differences.
is a hypersensitivity (allergic) reaction to abacavir causing fever and rash.
is a rare genetic disorder affecting development and multiple body systems.
is a bulge in the abdominal aorta that can rupture.