Adams-Oliver syndrome

syndrome characterized by defects of the scalp (aplasia cutis congenita), abnormalities of the fingers, toes, arms and legs
MedicalCondition rare_disease Q351708
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Adams-Oliver syndrome

Summary

Adams-Oliver syndrome is a rare disease[1]. It draws 33 Wikipedia views per month (rare_disease category, ranking #217 of 627).[2]

Key Facts

  • Adams-Oliver syndrome's instance of is recorded as rare disease[3].
  • Adams-Oliver syndrome's instance of is recorded as class of disease[4].
  • Forrest H. Adams is named after Adams-Oliver syndrome[5].
  • Adams-Oliver syndrome's subclass of is recorded as syndrome[6].
  • Adams-Oliver syndrome's MeSH descriptor ID is recorded as C538225[7].
  • Adams-Oliver syndrome's OMIM ID is recorded as 100300[8].
  • Adams-Oliver syndrome's OMIM ID is recorded as 614219[9].
  • Adams-Oliver syndrome's OMIM ID is recorded as 614814[10].
  • Adams-Oliver syndrome's OMIM ID is recorded as 615297[11].
  • Adams-Oliver syndrome's OMIM ID is recorded as 616028[12].
  • Adams-Oliver syndrome's DiseasesDB is recorded as 32741[13].
  • Adams-Oliver syndrome's Freebase ID is recorded as /m/09w89x[14].
  • Adams-Oliver syndrome's KEGG ID is recorded as H01413[15].
  • Adams-Oliver syndrome's Disease Ontology ID is recorded as DOID:0060227[16].
  • Adams-Oliver syndrome's Orphanet ID is recorded as 974[17].
  • Adams-Oliver syndrome's BBC Things ID is recorded as ee12a9de-9f7d-409f-a7a3-a36cf9b5f51e[18].
  • Adams-Oliver syndrome's ICD-9-CM is recorded as 759.89[19].
  • Adams-Oliver syndrome's health specialty is recorded as pediatrics[20].
  • Adams-Oliver syndrome's health specialty is recorded as dermatology[21].
  • Adams-Oliver syndrome's health specialty is recorded as orthopedics[22].
  • Adams-Oliver syndrome's genetic association is recorded as EOGT[23].
  • Adams-Oliver syndrome's genetic association is recorded as RBPJ[24].
  • Adams-Oliver syndrome's genetic association is recorded as DLL4[25].
  • Adams-Oliver syndrome's genetic association is recorded as NOTCH1[26].
  • Adams-Oliver syndrome's genetic association is recorded as DOCK6[27].

Why It Matters

Adams-Oliver syndrome draws 33 Wikipedia views per month (rare_disease category, ranking #217 of 627).[2] It has Wikipedia articles in 8 language editions, a strong signal of global cultural recognition.[28] It is known by 9 alternative names across languages and contexts.[29]

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] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  6. [8] . Disease Ontology. Retrieved . wikidata.org.
  7. [9] . Disease Ontology. Retrieved . wikidata.org.
  8. [10] . Disease Ontology. Retrieved . wikidata.org.
  9. [11] . Disease Ontology. Retrieved . wikidata.org.
  10. [12] . Disease Ontology. Retrieved . wikidata.org.
  11. [13] . wikidata.org.
  12. [14] . Freebase Data Dumps. wikidata.org.
  13. [15] . wikidata.org.
  14. [16] . Disease Ontology. Retrieved . wikidata.org.
  15. [17] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  16. [18] . BBC Things. wikidata.org.
  17. [19] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  18. [20] . wikidata.org.
  19. [21] . wikidata.org.
  20. [22] . wikidata.org.
  21. [23] . Mutations in EOGT confirm the genetic heterogeneity of autosomal-recessive Adams-Oliver syndrome. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  22. [24] . RBPJ mutations identified in two families affected by Adams-Oliver syndrome. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  23. [25] . Heterozygous Loss-of-Function Mutations in DLL4 Cause Adams-Oliver Syndrome. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  24. [26] . Mutations in NOTCH1 cause Adams-Oliver syndrome. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  25. [27] . Recessive mutations in DOCK6, encoding the guanidine nucleotide exchange factor DOCK6, lead to abnormal actin cytoskeleton organization and Adams-Oliver syndrome. Retrieved . platform.opentargets.org. Provenance: wikidata.org.

Class ancestry

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

Aggregate / graph-position facts

  1. [2] . Wikimedia Foundation. dumps.wikimedia.org.
  2. [28] . Wikidata sitelinks. wikidata.org.
  3. [29] . 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). Adams-Oliver syndrome. Retrieved May 3, 2026, from https://4ort.xyz/entity/adams-oliver-syndrome
MLA “Adams-Oliver syndrome.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/adams-oliver-syndrome.
BibTeX @misc{4ortxyz_adams-oliver-syndrome_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Adams-Oliver syndrome}}, year = {2026}, url = {https://4ort.xyz/entity/adams-oliver-syndrome}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Adams-Oliver syndrome — https://4ort.xyz/entity/adams-oliver-syndrome (retrieved 2026-05-03)

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