Androgen insensitivity syndrome
ICD-10 Code
E34.5
Androgen insensitivity syndrome
Definition
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).
Also known as androgen insensitivity syndrome, androgen insensitivity, X-linked recessive, androgen resistance syndrome, Goldberg-Maxwell syndrome, Morris syndrome, testicular feminization syndrome — per MONDO
Also identified as
- DOID 4674 per MONDO
- ICD10CM E34.5 per MONDO
- ICD9 259.5 per MONDO
- ICD9 259.51 per MONDO
- ICD9 259.8 per MONDO
- MESH D013734 per MONDO
- NCIT C27226 per MONDO
- OMIM 300068 per MONDO
- Orphanet 754 per MONDO
- SCTID 12313004 per MONDO
- UMLS C0039585 per MONDO
Affected Organs
| Organ | Involvement | Source |
|---|---|---|
| Endocrine gland | Disease Has Associated Anatomic Site | NCIT · CC BY 4.0 |