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renal agenesis

congenital disorder of urinary system
Class type of: kidney disease, renal hypoplasia Q669435

Facts

8 properties
Instance of
rare disease, class of disease[2]
Subclass of
kidney disease, renal hypoplasia[3][4]
Age of onset
any age, congenital onset[9][10]
Genetic association
ITGA8, HNF1B[7][8]
Has phenotype
multicystic dysplastic kidney, chronic renal insufficiency, urinary tract infection, urinary incontinence, ureterocele, vesicoureteral reflux, kidney failure, nephromegaly, hydronephrosis, arterial hypertension, oligohydramnios, abdominal pain, pyelonephritis, Moderate proteinuria, flank pain, abdominal mass, pelvic mass, vesicovaginal fistula, posterior urethral valve[12][13][14][15][16][17][18][19][20][21][22][23][24][25]
Health specialty
medical genetics[6]
NCI Thesaurus ID
C99041[5]
On focus list of Wikimedia project
WikiProject Medicine[11]
🏷️ Also known as
en hereditary urogenital adysplasia en renal hypoplasia en renal aplasia en renal agenesis en renal adysplasia en hereditary renal aplasia ar غياب الكلية الخلقي cs renální ageneze cs ageneze ledvin de Nierenagenesie el Νεφρική αγενεσία es Agenesia renal fr aplasie rénale fr agénésie rénale fr petit rein id Agenesis ginjal it agenesia renale nl nierhypoplasie pl Agenezja nerek tr Konjenital böbrek anomalileri
🔖 Identifiers · 20
OpenAlex ID
C2781218831
Disease Ontology ID
DOID:14766
DiseasesDB
11252
Exact match
purl.obolibrary.org, identifiers.org, www.orpha.net
Freebase ID
/m/03k3gv
GARD rare disease ID
9228
Human Phenotype Ontology ID
HP:0000104
ICD-10 ID
Q60.2
ICD-11 ID (Foundation)
683319223
ICD-11 ID (MMS)
LB30.00
ICD-9 ID
753.0
JSTOR topic ID (archived)
renal-agenesis
Show all 20 identifiers +8
KBpedia ID
RenalAgenesis
Medical Dictionary for Regulatory Activities ID
10038354
Microsoft Academic ID (discontinued)
2781218831
OMIM ID
191830
Orphanet ID
93108
Raras disease ID
D93108
UniProt disease ID
DI-02253
WikiProjectMed ID
Kidney agenesis

Report an error or request removal Lineage (PROV-JSON)

🔗 Connections
Subclass of 2
kidney disease, renal hypoplasia
Subtypes 2
Potter's syndrome, OHVIRA
Health specialty 1
medical genetics
Instance of 1
rare disease
On focus list of Wikimedia project 1
WikiProject Medicine
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Summary

renal agenesis is a rare disease[1].

References

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

Direct Wikidata claims

  1. [2] ↑ . wikidata.org.
  2. [3] ↑ . Disease Ontology. Retrieved . wikidata.org.
  3. [4] ↑ . wikidata.org.
  4. [5] ↑ . wikidata.org.
  5. [6] ↑ . wikidata.org.
  6. [7] ↑ . Integrin alpha 8 recessive mutations are responsible for bilateral renal agenesis in humans. wikidata.org.
  7. [8] ↑ . Retrieved . wikidata.org.
  8. [9] ↑ . Retrieved . wikidata.org.
  9. [10] ↑ . Retrieved . wikidata.org.
  10. [11] ↑ . wikidata.org.
  11. [12] ↑ . Retrieved . wikidata.org.
  12. [13] ↑ . Retrieved . wikidata.org.
  13. [14] ↑ . Retrieved . wikidata.org.
  14. [15] ↑ . Retrieved . wikidata.org.
  15. [16] ↑ . Retrieved . wikidata.org.
  16. [17] ↑ . Retrieved . wikidata.org.
  17. [18] ↑ . Retrieved . wikidata.org.
  18. [19] ↑ . Retrieved . wikidata.org.
  19. [20] ↑ . Retrieved . wikidata.org.
  20. [21] ↑ . Retrieved . wikidata.org.
  21. [22] ↑ . Retrieved . wikidata.org.
  22. [23] ↑ . Retrieved . wikidata.org.
  23. [24] ↑ . Retrieved . wikidata.org.
  24. [25] ↑ . Retrieved . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. 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). renal agenesis. Retrieved November 10, 2026, from https://4ort.xyz/entity/renal-agenesis
MLA “renal agenesis.” 4ort.xyz Knowledge Graph, 4ort.xyz, 10 Nov. 2026, https://4ort.xyz/entity/renal-agenesis.
BibTeX @misc{4ortxyz_renal-agenesis_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{renal agenesis}}, year = {2026}, url = {https://4ort.xyz/entity/renal-agenesis}, note = {Accessed: 2026-11-10}}
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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. 18d ago · ACorrêa (WMB) · 2026-10-24 view diff on Wikidata ↗
    Genetic association → ITGA8, HNF1B
    Age of onset → any age, congenital onset
    Has phenotype → multicystic dysplastic kidney, chronic renal insufficiency, urinary tract infection +1
    Raras disease ID → D93108
    "Changed the item: QuickStatements 3.0 batch #61469: Raras.org data import"
  2. 28d ago · VGMaintenanceBot bot · 2026-10-13 view diff on Wikidata ↗
    "Added qualifier: MediaWiki page ID: 1657, Add qualifier to WikiProjectMed ID `Kidney agenesis`"
  3. 5w ago · عُثمان · 2026-10-04 view diff on Wikidata ↗
    Human Phenotype Ontology ID → HP:0000104
    "Created claim: Human Phenotype Ontology ID: HP:0000104, Matched to Renal agenesis (#19255113) in HPO #mix'n'matc"
  4. 18w ago · JhealdBatch bot · 2026-07-05 view diff on Wikidata ↗
    On focus list of Wikimedia project → WikiProject Medicine
    Health specialty → medical genetics
    Subclass of → kidney disease, renal hypoplasia
    Genetic association → ITGA8, HNF1B
    + 1 other property edited (see Wikidata diff for full list)
    "Changed the item: QuickStatements 3.0 batch #39953: deprecate redundant disease superclasses (2)"
Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.