46 XX gonadal dysgenesis
gonadal dysgenesis that is characterized by the lack of functional ovaries to induce puberty in an otherwise 46,XX female
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Summary
46 XX gonadal dysgenesis is a class of disease[1]. It draws 701 Wikipedia views per month (class of disease category, ranking #564 of 1,968).[2]
Key Facts
- Subclass of: gonadal dysgenesis[3]
- Medical condition: medical genetics[4]
- NCI Thesaurus ID: C120197[5]
- Health specialty: medical genetics[6]
- Genetic association: FSHR[7], BMP15[8], HROB[9], BNC1[10], ESR2[11], MSH4[12], NR5A1[13], WNT4[14], MRPS22[15], PSMC3IP[16], FIGLA[17], ZSWIM7[18], SOHLH1[19], SPIDR[20]
- Age of onset: juvenile onset[21], adult onset[22]
- Exact match: http://purl.obolibrary.org/obo/DOID_14450[23], http://identifiers.org/doid/DOID:14450[24], http://www.orpha.net/ORDO/Orphanet_243[25]
- On focus list of Wikimedia project: WikiProject Medicine[26]
- Has phenotype: Q141815004[27], Delayed skeletal maturation[28], Q141815870[29], short stature[30]
- P14914: D00243[31]
Why It Matters
46 XX gonadal dysgenesis has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.[32] It is known by 18 alternative names across languages and contexts.[33]