Androgen insensitivity syndrome ( AIS ) is a condition characterized by the inability to respond to androgens, usually due to androgen...

Androgen deficiency is a medical condition marked by inadequate androgenic activity in the body. It most often affects women and is also...

Ablepharon macrostomia syndrome ( AMS ) is an extremely rare autosomal dominant genetic disorder marked by unusual phenotypic features...

Aarskog–Scott syndrome ( AAS ) is a rare disorder inherited in an X-linked manner and is marked by short stature, facial abnormalities,...

TS 45,X/46,XY mosaicism , also referred to as X0/XY mosaicism and mixed gonadal dysgenesis , is a variation in human sex development...

17β-Hydroxysteroid dehydrogenase III deficiency is a rare autosomal recessive disorder of sexual development that leads to 46,XY...

5α-Reductase 2 deficiency (5αR2D) is an autosomal recessive disorder resulting from mutations that disrupt the function of SRD5A2 , a...