46,XX disorder of sex development
46,XX disorder of sex development
Definition
Conditions affecting individuals with 46,XX karyotype characterized by atypical development of one or more of the following: the gonads, the internal reproductive structures, the external reproductive/genital structures.
Also known as 46,XX differences of Sex development, 46,XX disorders of Sex development, 46,XX DSD, female pseudohermaphroditism — per MONDO
Also identified as
- MESH D058489 per MONDO
- NCIT C127169 per MONDO
- Orphanet 2982 per MONDO
- SCTID 8800006 per MONDO
- UMLS C2936403 per MONDO
Affected Organs
| Organ | Involvement | Source |
|---|---|---|
| Genitourinary system | Disease Has Associated Anatomic Site | NCIT · CC BY 4.0 |
| Genitourinary system | Disease Has Primary Anatomic Site | NCIT · CC BY 4.0 |
| Reproductive system | Disease Has Associated Anatomic Site | NCIT · CC BY 4.0 |
| Reproductive system | Disease Has Primary Anatomic Site | NCIT · CC BY 4.0 |