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Parent Node:
expand46,XX disorder of gonadal development (MONDO:0017961)
Parent Node:
expandfemale infertility due to gonadal dysgenesis (MONDO:0018402)
Parent Node:
expandgenetic infertility (MONDO:0017143)
Parent Node:
expandgonadal dysgenesis (MONDO:0001967)
Parent Node:
expandgonadal dysgenesis of gynecological interest (MONDO:0020038)
Parent Node:
expandinherited primary ovarian failure (MONDO:0019852)
..Starting node
..expand46 XX gonadal dysgenesis ()

       Child Nodes:
........expand46,XX testicular disorder of sex development ()
........expandovarian dysgenesis 1 ()
........expandovarian dysgenesis 2 ()
........expandovarian dysgenesis 3 ()
........expandovarian dysgenesis 5 ()
........expandovarian dysgenesis 6 ()
........expandovarian dysgenesis 7 ()
........expandSERKAL syndrome ()



 Sister Nodes: 
..expand46 XX gonadal dysgenesis ()
..expand46,XX ovarian dysgenesis-short stature syndrome ()
..expandaromatase deficiency ()
..expandataxia telangiectasia ()
..expandblepharophimosis, ptosis, and epicanthus inversus syndrome ()
..expandclassic galactosemia ()
..expandcongenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency ()
..expandcongenital lipoid adrenal hyperplasia due to STAR deficency ()
..expandmicrocephalic primordial dwarfism-insulin resistance syndrome ()
..expandosteosclerosis-ichthyosis-premature ovarian failure syndrome ()
..expandPerrault syndrome ()
..expandpremature ovarian failure 1 ()
..expandpremature ovarian failure 11 ()
..expandpremature ovarian failure 12 ()
..expandpremature ovarian failure 2A ()
..expandpremature ovarian failure 2B ()
..expandpremature ovarian failure 3 ()
..expandpremature ovarian failure 5 ()
..expandpremature ovarian failure 6 ()
..expandpremature ovarian failure 7 ()
..expandpremature ovarian failure 8 ()
..expandpremature ovarian failure 9 ()
..expandSatoyoshi syndrome ()
..expandtetrasomy X ()
..expandtrisomy X ()
..expandTurner syndrome ()
..expandX small rings ()
   

MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Term ID:9299
Name:46 XX gonadal dysgenesis
Definition:46,XX gonadal dysgenesis (46,XX GD) is a primary ovarian defect leading to premature ovarian failure (POF; see this term) in otherwise normal 46,XX females as a result of failure of the gonads to develop or due to resistance to gonadotrophin stimulation.
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Synonyms:46,XX complete gonadal dysgenesis; 46,XX gonadal dysgenesis; 46,XX ovarian dysgenesis; 46,XX pure gonadal dysgenesis; follicular stimulating hormone-resistant ovaries; FSH-RO; hypergonadotropic ovarian dysgenesis; ovarian dysgenesis; XX female gonadal dysgenesis; XX gonadal dysgenesis; XX-GD
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Reference: MedGen:
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