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 atypical sex development from impaired testosterone production.
is a genetic condition affecting hormone production, sex development, and adrenal function.
is a genetic condition with reduced androgen production, affecting sex development.
is a genetic condition from 17,20-lyase deficiency, reducing sex hormones.
causes impaired testosterone production, atypical genital development, and delayed puberty in 46,XY.
is a genetic condition causing reduced testosterone production and atypical genital development.
is a 46,XY sex development difference from prenatal endocrine disruptor exposure.
is a group of hormone-related conditions affecting 46,XY sex development.
is a group of conditions causing variations in 46,XY sex development.
is a rare genetic disorder affecting sex development and adrenal hormones.
is a genetic condition affecting XY sex development from impaired dihydrotestosterone production.
is a condition where XY chromosomes lead to atypical gonadal development.
is a rare genetic condition causing underdeveloped gonads and progressive nerve damage.
is a rare condition with both ovarian and testicular tissue, affecting development.
is a 46,XY difference in sex development with underdeveloped testes, ambiguous genitalia.
is a difference in sex development causing female or underdeveloped male features.
is a genetic sex development difference causing typical female development in 46,XY.
is a genetic difference in sex development (DSD) affecting XY individuals.
is a genetic condition affecting gonadal development in people with XY chromosomes.
is a genetic condition affecting sex development in people with XY chromosomes.
is a genetic condition disrupting sex development in 46,XY individuals.
is a rare genetic condition causing atypical sex development in XY individuals.
is a rare difference in sex development affecting people with XY chromosomes.
is a rare genetic difference in sex development causing atypical gonadal development.