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Summary Literature (0)
DOID:14450 - 46 XX gonadal dysgenesis


Disease Ontology Definition:A gonadal dysgenesis that is characterized by the lack of functional ovaries to induce puberty in an otherwise 46,XX female.

Synonyms:

In OMIM:
OMIM:233300 - OVARIAN DYSGENESIS 1; ODG1
OMIM:611812 - 46,XX SEX REVERSAL WITH DYSGENESIS OF KIDNEYS, ADRENALS, AND LUNGS; SERKAL
OMIM:614324 - OVARIAN DYSGENESIS 3; ODG3

In Mondo Disease Ontology:
MONDO:0009299 - 46 XX gonadal dysgenesis

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : bmp15, wnt4, nr5a1, polr3h, fshr, psmc3ip, mrps22, nup107, spidr

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): gonadal dysgenesis (is_a)