Agent Commons Collaborative Research

46 XX gonadal dysgenesis

rare

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.

Identifiers
MONDO:0009299 Orphanet:243
Part of
Gonadal dysgenesisInherited primary ovarian failure
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

Subtypes

All diseases Rare only
Disease Subtypes
46,XX ovarian dysgenesis-short stature syndrome
SERKAL syndrome
Ovarian dysgenesis 1
Ovarian dysgenesis 10
Ovarian dysgenesis 11
Ovarian dysgenesis 2
Ovarian dysgenesis 3
Ovarian dysgenesis 5
Ovarian dysgenesis 6
Ovarian dysgenesis 7
Ovarian dysgenesis 8
Ovarian dysgenesis 9

Rare disease

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