growth hormone deficiency

human disease
MedicalCondition rare_disease Q369262
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Summary

growth hormone deficiency is a rare disease[1]. It draws 180 Wikipedia views per month (rare_disease category, ranking #81 of 627).[2]

Key Facts

  • growth hormone deficiency's instance of is recorded as rare disease[3].
  • growth hormone deficiency's instance of is recorded as class of disease[4].
  • growth hormone deficiency is a type of dwarfism[5].
  • growth hormone deficiency's NCI Thesaurus ID is recorded as C34555[6].
  • growth hormone deficiency's health specialty is recorded as endocrinology[7].
  • growth hormone deficiency's genetic association is recorded as GH1[8].
  • growth hormone deficiency's exact match is recorded as http://identifiers.org/doid/DOID:9405[9].
  • growth hormone deficiency's exact match is recorded as http://purl.obolibrary.org/obo/DOID_9405[10].
  • growth hormone deficiency's on focus list of Wikimedia project is recorded as WikiProject Medicine[11].

Why It Matters

growth hormone deficiency draws 180 Wikipedia views per month (rare_disease category, ranking #81 of 627).[2] It has Wikipedia articles in 15 language editions, a strong signal of global cultural recognition.[12] It is known by 27 alternative names across languages and contexts.[13]

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] ↑ . wikidata.org.
  4. [6] ↑ . Disease Ontology. Retrieved . wikidata.org.
  5. [7] ↑ . wikidata.org.
  6. [8] ↑ . Genetic basis of endocrine disease. 6. Molecular basis of familial human growth hormone deficiency. wikidata.org.
  7. [9] ↑ . Identifiers.org. registry.identifiers.org. Provenance: wikidata.org.
  8. [10] ↑ . Disease Ontology. Retrieved . wikidata.org.
  9. [11] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] ↑ . Wikimedia Foundation. dumps.wikimedia.org.
  2. [12] ↑ . Wikidata sitelinks. wikidata.org.
  3. [13] ↑ . 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). growth hormone deficiency. Retrieved October 14, 2026, from https://4ort.xyz/entity/growth-hormone-deficiency
MLA “growth hormone deficiency.” 4ort.xyz Knowledge Graph, 4ort.xyz, 14 Oct. 2026, https://4ort.xyz/entity/growth-hormone-deficiency.
BibTeX @misc{4ortxyz_growth-hormone-deficiency_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{growth hormone deficiency}}, year = {2026}, url = {https://4ort.xyz/entity/growth-hormone-deficiency}, note = {Accessed: 2026-10-14}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): growth hormone deficiency — https://4ort.xyz/entity/growth-hormone-deficiency (retrieved 2026-10-14)

Canonical URL: https://4ort.xyz/entity/growth-hormone-deficiency · 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. 11d ago · عُثمان · 2026-10-04 view diff on Wikidata ↗
    Sitelink count → 23
    Wikipedia languages → ['ar', 'de', 'el', 'en', 'es', 'eu', 'fa', 'fr', 'hi', 'hy', 'it', 'ja', 'nl', '
    Human phenotype ontology id → HP:0000824
    Claims rich → —
    "/* wbsetclaim-create:1||1 */ Human phenotype ontology id: HP:0000824, Matched to [[:toollabs:mix-n-match/#/entry/19252515|Growth hormone deficiency (#19252515)]] in [[:toollabs:mix-n-match/#/catalog/4"
  2. 9w ago · Infovarius · 2026-08-08 view diff on Wikidata ↗
    Image → —
    Related image → Somatotropine.GIF
    Wikidata description → human disease
    "/* wbeditentity-statements-multiple-properties-update:0||2 */ Moving Image to Related image"
  3. 14w ago · JhealdBatch bot · 2026-07-04 view diff on Wikidata ↗
    Instance of → rare disease, class of disease
    "/* wbeditentity-update:0| */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/39873|batch #39873]]: P31 = "type of disease""
  4. 18w ago · Trade · 2026-06-09 view diff on Wikidata ↗
    Image → —
    "/* wbsetclaim-create:2||1 */ Image: Somatotropine.GIF"
  5. 21w ago · InternetArchiveBot bot · 2026-05-18 view diff on Wikidata ↗
    Subclass of → dwarfism
    Instance of → —
    Instance of → rare disease, class of disease
    Disease ontology id → DOID:9405
    + 6 other properties edited (see Wikidata diff for full list)
    "/* wbsetclaim-update-references:1||1|2 */ Openalex id: C2779952775, Rescuing 1 sources and submitting 0 for archiving. #IABot (v2.0.9.5)"
Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.