premature ovarian failure

ovarian disease where ovaries do not produce estrogen despite high levels of circulating gonadotropins in women under 40
MedicalCondition rare_disease Q647630
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premature ovarian failure

Summary

premature ovarian failure is a rare disease[1]. It draws 122 Wikipedia views per month (rare_disease category, ranking #165 of 627).[2]

Key Facts

  • premature ovarian failure's instance of is recorded as rare disease[3].
  • premature ovarian failure's instance of is recorded as class of disease[4].
  • premature ovarian failure is a type of ovarian disease[5].
  • premature ovarian failure is a type of poor ovarian reserve[6].
  • premature ovarian failure is a type of disease[7].
  • premature ovarian failure's NCI Thesaurus ID is recorded as C113352[8].
  • premature ovarian failure's health specialty is recorded as endocrinology[9].
  • premature ovarian failure's drug or therapy used for treatment is recorded as ethinylestradiol[10].
  • premature ovarian failure's drug or therapy used for treatment is recorded as 17β-estradiol[11].
  • premature ovarian failure's drug or therapy used for treatment is recorded as estropipate[12].
  • premature ovarian failure's genetic association is recorded as HFM1[13].
  • premature ovarian failure's genetic association is recorded as FMR1[14].
  • premature ovarian failure's genetic association is recorded as STAG3[15].
  • premature ovarian failure's genetic association is recorded as NOBOX[16].
  • premature ovarian failure's genetic association is recorded as NR5A1[17].
  • premature ovarian failure's genetic association is recorded as POF1B[18].
  • premature ovarian failure's genetic association is recorded as DIAPH2[19].
  • premature ovarian failure's genetic association is recorded as FOXL2[20].
  • premature ovarian failure's genetic association is recorded as FIGLA[21].
  • premature ovarian failure's exact match is recorded as http://purl.obolibrary.org/obo/DOID_5426[22].
  • premature ovarian failure's exact match is recorded as http://identifiers.org/doid/DOID:5426[23].
  • premature ovarian failure's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_619[24].
  • premature ovarian failure's on focus list of Wikimedia project is recorded as WikiProject Medicine[25].

Why It Matters

premature ovarian failure draws 122 Wikipedia views per month (rare_disease category, ranking #165 of 627).[2] It has Wikipedia articles in 16 language editions, a strong signal of global cultural recognition.[26] It is known by 16 alternative names across languages and contexts.[27]

References

Programmatic citations — every numbered marker resolves to a verifiable graph row below.

Direct Wikidata claims

  1. [3] . wikidata.org.
  2. [4] . wikidata.org.
  3. [5] . Disease Ontology. Retrieved . wikidata.org.
  4. [6] . wikidata.org.
  5. [7] . wikidata.org.
  6. [8] . Disease Ontology. Retrieved . wikidata.org.
  7. [9] . wikidata.org.
  8. [10] . NDF-RT. Retrieved . wikidata.org.
  9. [11] . NDF-RT. Retrieved . wikidata.org.
  10. [12] . NDF-RT. Retrieved . wikidata.org.
  11. [13] . Mutations in HFM1 in Recessive Primary Ovarian Insufficiency. wikidata.org.
  12. [14] . Studies of FRAXA and FRAXE in women with premature ovarian failure. wikidata.org.
  13. [15] . Mutant Cohesin in Premature Ovarian Failure. wikidata.org.
  14. [16] . NOBOX homeobox mutation causes premature ovarian failure. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  15. [17] . Mutations in NR5A1 associated with ovarian insufficiency. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  16. [18] . Disruption of POF1B binding to nonmuscle actin filaments is associated with premature ovarian failure. wikidata.org.
  17. [19] . A human homologue of the Drosophila melanogaster diaphanous gene is disrupted in a patient with premature ovarian failure: evidence for conserved function in oogenesis and implications for human sterility. wikidata.org.
  18. [20] . Identification of novel mutations in FOXL2 associated with premature ovarian failure. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  19. [21] . Transcription factor FIGLA is mutated in patients with premature ovarian failure. wikidata.org.
  20. [22] . Disease Ontology. Retrieved . wikidata.org.
  21. [23] . Identifiers.org. registry.identifiers.org. Provenance: wikidata.org.
  22. [24] . wikidata.org.
  23. [25] . wikidata.org.

Class ancestry

  1. [1] . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] . Wikimedia Foundation. dumps.wikimedia.org.
  2. [26] . Wikidata sitelinks. wikidata.org.
  3. [27] . Wikidata aliases. wikidata.org.

📑 Cite this page

Use these citations when quoting this entity in research, articles, AI prompts, or wherever provenance matters. We aggregate Wikidata + Wikipedia + authoritative open-data sources; the stitched, scored, cross-referenced view is what 4ort.xyz contributes.

APA 4ort.xyz Knowledge Graph. (2026). premature ovarian failure. Retrieved May 3, 2026, from https://4ort.xyz/entity/premature-ovarian-failure
MLA “premature ovarian failure.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/premature-ovarian-failure.
BibTeX @misc{4ortxyz_premature-ovarian-failure_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{premature ovarian failure}}, year = {2026}, url = {https://4ort.xyz/entity/premature-ovarian-failure}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): premature ovarian failure — https://4ort.xyz/entity/premature-ovarian-failure (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/premature-ovarian-failure · Last refreshed:

Edit History

Rolling log of changes to this entity's Wikidata record. Values shown reflect the current state of each edited property — follow the history link to see the precise diff for any edit.

  1. 28d ago · Mowsenter · 2026-05-10 view diff on Wikidata ↗
    On focus list of wikimedia project WikiProject Medicine
    Health specialty endocrinology
    Subclass of
    Instance of
    + 5 other properties edited (see Wikidata diff for full list)
    "/* wbsetreference-add:2| */ [[Property:P672]]: C19.391.630.750"
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