asthenozoospermia

medical term for reduced sperm motility
MedicalCondition rare_disease Q2329041
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asthenozoospermia

Summary

asthenozoospermia is a rare disease[1]. asthenozoospermia draws 83 Wikipedia views per month (rare_disease category, ranking #191 of 627).[2]

Key Facts

  • asthenozoospermia's instance of is recorded as rare disease[3].
  • asthenozoospermia's instance of is recorded as class of disease[4].
  • asthenozoospermia is a type of male infertility[5].
  • asthenozoospermia's Commons category is recorded as Asthenozoospermia[6].
  • asthenozoospermia's health specialty is recorded as urology[7].
  • asthenozoospermia's genetic association is recorded as SLC26A8[8].
  • asthenozoospermia's genetic association is recorded as CATSPER1[9].
  • asthenozoospermia's genetic association is recorded as SEPTIN12[10].
  • asthenozoospermia's genetic association is recorded as DNAH1[11].
  • asthenozoospermia's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_276234[12].

Why It Matters

asthenozoospermia draws 83 Wikipedia views per month (rare_disease category, ranking #191 of 627).[2] asthenozoospermia has Wikipedia articles in 11 language editions, a strong signal of global cultural recognition.[13] asthenozoospermia is known by 7 alternative names across languages and contexts.[14]

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] . wikidata.org.
  4. [6] . wikidata.org.
  5. [7] . wikidata.org.
  6. [8] . Missense mutations in SLC26A8, encoding a sperm-specific activator of CFTR, are associated with human asthenozoospermia. wikidata.org.
  7. [9] . Human male infertility caused by mutations in the CATSPER1 channel protein. wikidata.org.
  8. [10] . SEPTIN12 genetic variants confer susceptibility to teratozoospermia. wikidata.org.
  9. [11] . Open Targets Platform. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  10. [12] . wikidata.org.

Class ancestry

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

Aggregate / graph-position facts

  1. [2] . Wikimedia Foundation. dumps.wikimedia.org.
  2. [13] . Wikidata sitelinks. wikidata.org.
  3. [14] . 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). asthenozoospermia. Retrieved May 3, 2026, from https://4ort.xyz/entity/asthenozoospermia
MLA “asthenozoospermia.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/asthenozoospermia.
BibTeX @misc{4ortxyz_asthenozoospermia_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{asthenozoospermia}}, year = {2026}, url = {https://4ort.xyz/entity/asthenozoospermia}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): asthenozoospermia — https://4ort.xyz/entity/asthenozoospermia (retrieved 2026-05-03)

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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. 8d ago · Twofivesixbot bot · 2026-05-28 view diff on Wikidata ↗
    Health specialty urology
    Genetic association SLC26A8, CATSPER1, SEPTIN12 +1
    Subclass of
    Subclass of male infertility
    + 3 other properties edited (see Wikidata diff for full list)
    "/* wbsetclaim-update-qualifiers:1||1|2 */ [[Property:P8189]]: 987007549464205171, mv to monolingual text names on J9U statements"
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