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.
results from excess androgens (male hormones) causing atypical genital development prenatally.
involves genital differences in 46,XX infants from maternal androgen exposure during pregnancy.
involves prenatal maternal androgen exposure causing genital masculinization in 46,XX individuals.
results from excess male hormones (androgens) before birth, affecting genital development.
is a female-chromosome condition from fetal-placental androgen excess, affecting genital development.
is prenatal exposure to maternal androgens, causing genital masculinization in 46,XX individuals.
causes atypical genital development and anorectal malformations in people with 46,XX.
is a rare genetic condition affecting sex development and skeletal formation.
is a rare condition affecting gonadal development, sex characteristics, puberty, and fertility.
is a rare genetic condition causing ovarian failure, absent puberty, infertility.
is a rare genetic disorder causing ovarian underdevelopment, short stature, infertility.
is a rare condition where ovarian and testicular tissues both develop.
is a genetic condition where XX individuals develop male characteristics, often infertile.
is a genetic DSD with testicular development in 46,XX individuals, often infertile.
is a genetic sex development condition causing male traits in XX individuals.
is a genetic disorder causing testicular development in 46,XX individuals.
is a rare genetic difference in sex development causing male phenotype.
is a rare condition with XX chromosomes and testicular development.
is a genetic sex development difference with nonworking gonads and infertility.
is a spectrum affecting sex development in people with XY chromosomes.
is a genetic enzyme deficiency reducing testosterone, altering 46,XY sex development.
is a genetic condition causing atypical genital development in 46,XY individuals.
is a genetic condition affecting sex development and cholesterol-derived hormone production.
is a genetic condition where tissues cannot properly convert testosterone.
