Home › Entities › rare_disease › hyperphenylalaninemia

hyperphenylalaninemia

medical condition
MedicalCondition rare_disease Q5898279
Press Enter · cited answer in seconds

hyperphenylalaninemia

Summary

hyperphenylalaninemia is a rare disease[1]. hyperphenylalaninemia has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.[2]

Key Facts

  • hyperphenylalaninemia's instance of is recorded as rare disease[3].
  • hyperphenylalaninemia's instance of is recorded as disease[4].
  • hyperphenylalaninemia is a type of metabolic disease[5].
  • hyperphenylalaninemia is a type of disorder of phenylalanine metabolism[6].
  • hyperphenylalaninemia's health specialty is recorded as endocrinology[7].
  • hyperphenylalaninemia's genetic association is recorded as QDPR[8].

Why It Matters

hyperphenylalaninemia has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.[2]

Related Entities

disease endocrinology

References

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

Direct Wikidata claims

  1. [3] ↑ . wikidata.org.
  2. [4] ↑ . New variant of phenylketonuria with progressive neurological illness unresponsive to phenylalanine restriction. wikidata.org.
  3. [5] ↑ . wikidata.org.
  4. [6] ↑ . wikidata.org.
  5. [7] ↑ . wikidata.org.
  6. [8] ↑ . Insertion of an extra codon for threonine is a cause of dihydropteridine reductase deficiency. 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). hyperphenylalaninemia. Retrieved May 3, 2026, from https://4ort.xyz/entity/hyperphenylalaninemia
MLA “hyperphenylalaninemia.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/hyperphenylalaninemia.
BibTeX @misc{4ortxyz_hyperphenylalaninemia_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{hyperphenylalaninemia}}, year = {2026}, url = {https://4ort.xyz/entity/hyperphenylalaninemia}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): hyperphenylalaninemia — https://4ort.xyz/entity/hyperphenylalaninemia (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/hyperphenylalaninemia · 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. 3d ago · JhealdBatch bot · 2026-07-04 view diff on Wikidata ↗
    Health specialty → endocrinology
    Subclass of → metabolic disease, disorder of phenylalanine metabolism
    Subclass of → —
    Genetic association → QDPR
    + 3 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/39873|batch #39873]]: P31 = "type of disease""
Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.