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hyperprolinemia

human disease
MedicalCondition rare_disease Q13637044
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hyperprolinemia

Summary

hyperprolinemia is a rare disease[1]. hyperprolinemia has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[2]

Key Facts

  • hyperprolinemia's instance of is recorded as rare disease[3].
  • hyperprolinemia's instance of is recorded as class of disease[4].
  • hyperprolinemia is a type of amino acid metabolic disorder[5].
  • hyperprolinemia is a type of inborn disorder of ornithine or proline metabolism[6].
  • hyperprolinemia's health specialty is recorded as medical genetics[7].
  • hyperprolinemia's genetic association is recorded as ALDH4A1[8].
  • hyperprolinemia's genetic association is recorded as PRODH[9].
  • hyperprolinemia's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_289866[10].
  • hyperprolinemia's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0080541[11].
  • hyperprolinemia's exact match is recorded as http://identifiers.org/doid/DOID:0080541[12].
  • hyperprolinemia's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].

Why It Matters

hyperprolinemia has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[2]

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] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  5. [7] ↑ . wikidata.org.
  6. [8] ↑ . Mutations in the Delta1-pyrroline 5-carboxylate dehydrogenase gene cause type II hyperprolinemia. wikidata.org.
  7. [9] ↑ . PRODH mutations and hyperprolinemia in a subset of schizophrenic patients. wikidata.org.
  8. [10] ↑ . wikidata.org.
  9. [11] ↑ . Disease Ontology. Retrieved . wikidata.org.
  10. [12] ↑ . Identifiers.org. registry.identifiers.org. Provenance: wikidata.org.
  11. [13] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] ↑ . Wikidata sitelinks. 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). hyperprolinemia. Retrieved May 3, 2026, from https://4ort.xyz/entity/hyperprolinemia
MLA “hyperprolinemia.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/hyperprolinemia.
BibTeX @misc{4ortxyz_hyperprolinemia_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{hyperprolinemia}}, year = {2026}, url = {https://4ort.xyz/entity/hyperprolinemia}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): hyperprolinemia — https://4ort.xyz/entity/hyperprolinemia (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/hyperprolinemia · 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. 1d ago · JhealdBatch bot · 2026-07-05 view diff on Wikidata ↗
    On focus list of wikimedia project → WikiProject Medicine
    Health specialty → medical genetics
    Subclass of → amino acid metabolic disorder, inborn disorder of ornithine or proline metabolism
    Subclass of → —
    + 4 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/39953|batch #39953]]: deprecate redundant disease superclasses (2)"
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