Home › Entities › developmental_defect_during_embryogenesis › renal hypomagnesemia 5 with ocular involvement

renal hypomagnesemia 5 with ocular involvement

human disease
MedicalCondition developmental_defect_during_embryogenesis Q32136710
Press Enter · cited answer in seconds

Summary

renal hypomagnesemia 5 with ocular involvement is a developmental defect during embryogenesis[1]. It is known by 17 alternative names across languages and contexts.[2]

Key Facts

  • Instance of: class of disease[3]
  • Subclass of: primary hypomagnesemia[4], oculocerebrorenal syndrome[5], colobomatous and areolar dystrophy[6], familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis[7], hereditary retinal dystrophy[8]
  • Genetic association: CLDN19[9]
  • Exact match: http://purl.obolibrary.org/obo/DOID_0060881[10], http://identifiers.org/doid/DOID:0060881[11]
  • On focus list of Wikimedia project: WikiProject Medicine[12]

References

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

Direct Wikidata claims

  1. [3] ↑ . wikidata.org.
  2. [4] ↑ . Disease Ontology. Retrieved . wikidata.org.
  3. [5] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  4. [6] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  5. [7] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  6. [8] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  7. [9] ↑ . UniProt. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  8. [10] ↑ . Disease Ontology. Retrieved . wikidata.org.
  9. [11] ↑ . Identifiers.org. registry.identifiers.org. Provenance: wikidata.org.
  10. [12] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] ↑ . 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). renal hypomagnesemia 5 with ocular involvement. Retrieved October 18, 2026, from https://4ort.xyz/entity/renal-hypomagnesemia-5-with-ocular-involvement
MLA “renal hypomagnesemia 5 with ocular involvement.” 4ort.xyz Knowledge Graph, 4ort.xyz, 18 Oct. 2026, https://4ort.xyz/entity/renal-hypomagnesemia-5-with-ocular-involvement.
BibTeX @misc{4ortxyz_renal-hypomagnesemia-5-with-ocular-involvement_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{renal hypomagnesemia 5 with ocular involvement}}, year = {2026}, url = {https://4ort.xyz/entity/renal-hypomagnesemia-5-with-ocular-involvement}, note = {Accessed: 2026-10-18}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): renal hypomagnesemia 5 with ocular involvement — https://4ort.xyz/entity/renal-hypomagnesemia-5-with-ocular-involvement (retrieved 2026-10-18)

Canonical URL: https://4ort.xyz/entity/renal-hypomagnesemia-5-with-ocular-involvement · 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. 15w ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Mondo id → MONDO_0009548
    Genetic association → CLDN19
    Gard rare disease id → 3451
    Orphanet id → 2196
    + 12 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"
Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.