46,XY complete gonadal dysgenesis

MONDO:0010765

46,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.

Also known as: 46 XY gonadal dysgenesis, 46, XY CGD, 46, XY complete gonadal dysgenesis, 46, XY pure gonadal dysgenesis, 46,XY CGD, 46,XY SEX reversal, 46,XY gonadal dysgenesis, 46,XY pure gonadal dysgenesis

9 clinical trials for this condition and its sub-types, 0 tagged with 46,XY complete gonadal dysgenesis itself.

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Where it sits in the disease tree

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Part of

↑ Disorder of development or morphogenesis (5188) ↑ Familial hypertrophic cardiomyopathy (86) ↑ Gonadal dysgenesis (32)

Sub-types of 46,XY complete gonadal dysgenesis

46,XY sex reversal 5 1 trial
46,XY disorder of sex development due to testicular 17,20-desmolase deficiency 0 trials
46,XY gonadal dysgenesis-motor and sensory neuropathy syndrome 0 trials
46,XY sex reversal 1 0 trials
46,XY sex reversal 10 0 trials
46,XY sex reversal 11 0 trials
46,XY sex reversal 2 0 trials
46,XY sex reversal 3 0 trials
46,XY sex reversal 4 0 trials
46,XY sex reversal 6 0 trials
46,XY sex reversal 7 0 trials
46,XY sex reversal 9 0 trials

Including sub-types (9) Tagged with 46,XY complete gonadal dysgenesis (0)

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