CAKUT

urinary system disease characterized by structural malformations in the kidney and/or urinary tract containing vesicoureteral reflux
MedicalCondition developmental_defect_during_embryogenesis Q30899323
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CAKUT

Summary

CAKUT is a developmental defect during embryogenesis[1]. CAKUT is known by 5 alternative names across languages and contexts.[2]

Key Facts

  • CAKUT's instance of is recorded as developmental defect during embryogenesis[3].
  • CAKUT's instance of is recorded as class of disease[4].
  • CAKUT is a type of urinary system disease[5].
  • CAKUT is a type of developmental defect during embryogenesis[6].
  • CAKUT's genetic association is recorded as genes associated with CAKUT[7].
  • CAKUT's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0080205[8].
  • CAKUT's exact match is recorded as http://identifiers.org/doid/DOID:0080205[9].
  • CAKUT's on focus list of Wikimedia project is recorded as WikiProject Medicine[10].

Why It Matters

CAKUT is known by 5 alternative names across languages and contexts.[2]

📑 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). CAKUT. Retrieved October 2, 2026, from https://4ort.xyz/entity/cakut
MLA “CAKUT.” 4ort.xyz Knowledge Graph, 4ort.xyz, 2 Oct. 2026, https://4ort.xyz/entity/cakut.
BibTeX @misc{4ortxyz_cakut_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{CAKUT}}, year = {2026}, url = {https://4ort.xyz/entity/cakut}, note = {Accessed: 2026-10-02}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): CAKUT — https://4ort.xyz/entity/cakut (retrieved 2026-10-02)

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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. 10w ago · KrBot bot · 2026-07-23 view diff on Wikidata ↗
    Subclass of → urinary system disease, developmental defect during embryogenesis
    "/* wbremoveclaims-remove:1| */ [[Property:P279]]: [[Q55788864]], дублирующееся значение / duplicate value"
  2. 13w ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Mondo id → MONDO_0019719
    Genetic association → genes associated with CAKUT
    Kegg id → H01867
    Orphanet id → 93545
    + 9 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/39742|batch #39742]]: subclass of disease, not instance"
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