Androgen insensitivity syndrome (AIS) is a disorder of sex development (DSD) characterized by the presence of female external genitalia, ambiguous genitalia or variable defects in virilization in a 46,XY individual with absent or partial responsiveness to age-appropriate levels of androgens. It comprises two clinical subgroups: complete AIS (CAIS) and partial AIS (PAIS). The disease is MONDO_0019154 (androgen insensitivity syndrome). Also known as: Goldberg - Maxwell syndrome, Goldberg-Maxwell syndrome, Morris syndrome, androgen insensitivity, X-linked recessive, androgen resistance syndrome, androgen-insensitivity syndrome, testicular feminization, testicular feminization syndrome.