46 XX gonadal dysgenesis

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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: ovarian dysgenesis,

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

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

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0009299 - Eumetazoa

MONDO:0009299 - Eumetazoa

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): gonadal dysgenesis (is_a)