46 XX gonadal dysgenesis
46 XX gonadal dysgenesis
Definition
46,XX gonadal dysgenesis (46,XX GD) is a primary ovarian defect leading to premature ovarian failure (POF) in otherwise normal 46,XX females as a result of failure of the gonads to develop or due to resistance to gonadotrophin stimulation.
Also known as 46,XX complete gonadal dysgenesis, 46,XX gonadal dysgenesis, 46,XX ovarian dysgenesis, 46,XX pure gonadal dysgenesis, follicular stimulating hormone-resistant ovaries, FSH-RO, hypergonadotropic ovarian dysgenesis, XX female gonadal dysgenesis, XX-GD — per MONDO
Also identified as
- DOID 14450 per MONDO
- MESH D023961 per MONDO
- NCIT C120197 per MONDO
- Orphanet 243 per MONDO
- SCTID 95198001 per MONDO
- UMLS C0685837 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 |
| Gonad | Disease Has Associated Anatomic Site | NCIT · CC BY 4.0 |
| Gonad | 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 |