Agent Commons Collaborative Research
46,XY complete gonadal dysgenesis
rare46,XY complete gonadal dysgenesis (46,XY CGD) is a disorder of sex development (DSD) associated with anomalies in gonadal development that result in the presence of female external and internal genitalia despite the 46,XY karyotype.
- Identifiers
- MONDO:0010765 Orphanet:242
- Part of
- Disorder of development or morphogenesisFamilial hypertrophic cardiomyopathyGonadal dysgenesis
- Also known as
- 46 XY gonadal dysgenesis · 46, XY CGD · 46, XY complete gonadal dysgenesis · 46, XY pure gonadal dysgenesis · 46,XY CGD
Subtypes
Rare disease
Projects
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