Lamb-Shaffer syndrome

human disease
MedicalCondition rare_disease Q55784997
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Lamb-Shaffer syndrome

Summary

Lamb-Shaffer syndrome is a rare disease[1]. It draws 12 Wikipedia views per month (rare_disease category, ranking #231 of 627).[2]

Key Facts

  • Lamb-Shaffer syndrome's instance of is recorded as rare disease[3].
  • Lamb-Shaffer syndrome's instance of is recorded as class of disease[4].
  • Lamb-Shaffer syndrome's subclass of is recorded as genetic disease[5].
  • Lamb-Shaffer syndrome's subclass of is recorded as genetic syndromic intellectual disability[6].
  • Lamb-Shaffer syndrome's OMIM ID is recorded as 616803[7].
  • Lamb-Shaffer syndrome's KEGG ID is recorded as H02156[8].
  • Lamb-Shaffer syndrome's Orphanet ID is recorded as 313892[9].
  • Lamb-Shaffer syndrome's health specialty is recorded as medical genetics[10].
  • Lamb-Shaffer syndrome's genetic association is recorded as SOX5[11].
  • Lamb-Shaffer syndrome's Google Knowledge Graph ID is recorded as /g/11gnrl_pj3[12].
  • Lamb-Shaffer syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_313892[13].
  • Lamb-Shaffer syndrome's UMLS CUI is recorded as C4225202[14].
  • Lamb-Shaffer syndrome's Mondo ID is recorded as MONDO_0017782[15].
  • Lamb-Shaffer syndrome's WikiProjectMed ID is recorded as Lamb-Shaffer syndrome[16].
  • Lamb-Shaffer syndrome's UniProt disease ID is recorded as DI-04646[17].

Why It Matters

Lamb-Shaffer syndrome draws 12 Wikipedia views per month (rare_disease category, ranking #231 of 627).[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] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  4. [6] . wikidata.org.
  5. [7] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  6. [8] . wikidata.org.
  7. [9] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  8. [10] . wikidata.org.
  9. [11] . Haploinsufficiency of SOX5 at 12p12.1 is associated with developmental delays with prominent language delay, behavior problems, and mild dysmorphic features. Retrieved . search.clinicalgenome.org. Provenance: wikidata.org.
  10. [12] . wikidata.org.
  11. [13] . wikidata.org.
  12. [14] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  13. [15] . wikidata.org.
  14. [16] . wikidata.org.
  15. [17] . wikidata.org.

Class ancestry

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

Aggregate / graph-position facts

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

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