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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:
Xenbase Genes
:
bmp15,
wnt4,
nr5a1,
polr3h,
fshr,
psmc3ip,
mrps22,
nup107,
spidr
| MONDO:0009299 - 46 XX gonadal dysgenesis |
| 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 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
gonadal dysgenesis (is_a)