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 an eyelid skin allergy from contact triggers causing redness, itching, swelling.
is immune-triggered inflammation of skin blood vessels causing rash and tenderness.
is an immune overreaction to harmless substances, causing symptoms and inflammation.
is an immune reaction causing sneezing, congestion, runny nose, itchy eyes.
is an allergic skin reaction causing itchy, raised welts (hives).
is a rare fungal infection affecting lungs, sinuses, skin, or brain.
is a severe brain malformation from failure of forebrain division.
is hair loss affecting scalp or body; causes and patterns vary.
is an immune deficiency linked to frequent infections and hair loss.
causes sudden, patchy hair loss when the immune system attacks follicles.
is an autoimmune condition causing complete scalp hair loss.
is an autoimmune condition causing complete body and scalp hair loss.
is a rare genetic disorder with alopecia, contractures, short stature, intellectual disability.
is a rare genetic disorder with alopecia, seizures, periodontitis, and intellectual disability.
is a rare genetic condition causing hair loss and intellectual disability.
is a rare genetic disorder with alopecia, intellectual disability, and hypogonadism.
is a rare genetic disorder with alopecia and intellectual disability.
is a rare genetic disorder causing hair loss (alopecia) and intellectual disability.
is a rare genetic disorder causing alopecia, developmental delay, and intellectual disability.
a rare genetic disorder causing hair loss (alopecia) and intellectual disability.
is an inherited disorder causing lung and liver disease from low AAT.
is a rare intestinal cancer of lymph cells causing malabsorption and diarrhea.
is a rare platelet storage pool disorder causing easy bruising and bleeding.
is a rare inherited platelet disorder causing easy bruising and bleeding.