PomBase home

Disease association ontology term - MONDO:0009299 - 46 XX gonadal dysgenesis

Term summary

ID
MONDO:0009299
Name
46 XX gonadal dysgenesis
Ontology or CV name
Disease association
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.

Parents

Annotation

Disease association

MONDO:0009299 - 46 XX gonadal dysgenesis

References:

Genes:

MONDO:0030736 - ovarian dysgenesis 10

References:

Genes:

MONDO:0013689 - ovarian dysgenesis 3

References:

Genes:

MONDO:0054850 - ovarian dysgenesis 6

References:

Genes: