focal dermal hypoplasia

form of ectodermal dysplasia
MedicalCondition developmental_defect_during_embryogenesis Q5463847
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focal dermal hypoplasia

Summary

focal dermal hypoplasia is a developmental defect during embryogenesis[1]. It draws 22 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #114 of 308).[2]

Key Facts

  • focal dermal hypoplasia's instance of is recorded as developmental defect during embryogenesis[3].
  • focal dermal hypoplasia's instance of is recorded as rare disease[4].
  • focal dermal hypoplasia's instance of is recorded as class of disease[5].
  • focal dermal hypoplasia's instance of is recorded as symptom or sign[6].
  • focal dermal hypoplasia is a type of ectodermal dysplasia[7].
  • focal dermal hypoplasia is a type of X-linked intellectual disability[8].
  • focal dermal hypoplasia is a type of malformation syndrome with hamartosis[9].
  • focal dermal hypoplasia is a type of connective tissue disease with eye involvement[10].
  • focal dermal hypoplasia is a type of lens shape anomaly[11].
  • focal dermal hypoplasia is a type of multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome[12].
  • focal dermal hypoplasia is a type of syndromic developmental defect of the eye[13].
  • focal dermal hypoplasia is a type of mixed dermis disorder[14].
  • focal dermal hypoplasia is a type of X-linked dominant disease[15].
  • focal dermal hypoplasia is a type of syndrome[16].
  • focal dermal hypoplasia's ICPC 2 ID is recorded as S83[17].
  • focal dermal hypoplasia's ICD-9-CM is recorded as 757.39[18].
  • focal dermal hypoplasia's NCI Thesaurus ID is recorded as C84715[19].
  • focal dermal hypoplasia's health specialty is recorded as medical genetics[20].
  • focal dermal hypoplasia's genetic association is recorded as PORCN[21].
  • focal dermal hypoplasia's exact match is recorded as http://purl.obolibrary.org/obo/DOID_2120[22].
  • focal dermal hypoplasia's exact match is recorded as http://identifiers.org/doid/DOID:2120[23].
  • focal dermal hypoplasia's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2092[24].
  • focal dermal hypoplasia's on focus list of Wikimedia project is recorded as WikiProject Medicine[25].

Why It Matters

focal dermal hypoplasia draws 22 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #114 of 308).[2] It has Wikipedia articles in 8 language editions, a strong signal of global cultural recognition.[26] It is known by 14 alternative names across languages and contexts.[27]

References

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

Direct Wikidata claims

  1. [3] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  2. [4] . wikidata.org.
  3. [5] . wikidata.org.
  4. [6] . wikidata.org.
  5. [7] . wikidata.org.
  6. [8] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  7. [9] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  8. [10] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  9. [11] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  10. [12] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  11. [13] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  12. [14] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  13. [15] . Disease Ontology. Retrieved . wikidata.org.
  14. [16] . Disease Ontology. Retrieved . wikidata.org.
  15. [17] . wikidata.org.
  16. [18] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  17. [19] . Disease Ontology. Retrieved . wikidata.org.
  18. [20] . wikidata.org.
  19. [21] . Q905695. Retrieved . search.clinicalgenome.org. Provenance: wikidata.org.
  20. [22] . Disease Ontology. Retrieved . wikidata.org.
  21. [23] . Identifiers.org. registry.identifiers.org. Provenance: wikidata.org.
  22. [24] . wikidata.org.
  23. [25] . wikidata.org.

Class ancestry

  1. [1] . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] . Wikimedia Foundation. dumps.wikimedia.org.
  2. [26] . Wikidata sitelinks. wikidata.org.
  3. [27] . 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). focal dermal hypoplasia. Retrieved May 3, 2026, from https://4ort.xyz/entity/focal-dermal-hypoplasia
MLA “focal dermal hypoplasia.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/focal-dermal-hypoplasia.
BibTeX @misc{4ortxyz_focal-dermal-hypoplasia_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{focal dermal hypoplasia}}, year = {2026}, url = {https://4ort.xyz/entity/focal-dermal-hypoplasia}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): focal dermal hypoplasia — https://4ort.xyz/entity/focal-dermal-hypoplasia (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/focal-dermal-hypoplasia · 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. 26d ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Subclass of ectodermal dysplasia, X-linked intellectual disability, malformation syndrome with hamartosis +7
    Health specialty medical genetics
    Genetic association PORCN
    Subclass of
    + 4 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.