syndromic intellectual disability

intellectual disability that is characterized by the presence of associated medical and behavioral sign and symptoms
MedicalCondition rare_disease Q18553536
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syndromic intellectual disability

Summary

syndromic intellectual disability is a rare disease[1].

Key Facts

  • syndromic intellectual disability's instance of is recorded as rare disease[2].
  • syndromic intellectual disability's instance of is recorded as class of disease[3].
  • syndromic intellectual disability's subclass of is recorded as intellectual disability[4].
  • syndromic intellectual disability's Commons category is recorded as Syndromes with intellectual disability[5].
  • syndromic intellectual disability's Disease Ontology ID is recorded as DOID:0050888[6].
  • syndromic intellectual disability's topic's main category is recorded as Category:Syndromes with intellectual disability[7].
  • syndromic intellectual disability's Orphanet ID is recorded as 102369[8].
  • syndromic intellectual disability's genetic association is recorded as SMS[9].
  • syndromic intellectual disability's genetic association is recorded as UBE2A[10].
  • syndromic intellectual disability's genetic association is recorded as OPHN1[11].
  • syndromic intellectual disability's genetic association is recorded as KIF1A[12].
  • syndromic intellectual disability's genetic association is recorded as AUTS2[13].
  • syndromic intellectual disability's genetic association is recorded as MED13L[14].
  • syndromic intellectual disability's genetic association is recorded as MYT1L[15].
  • syndromic intellectual disability's genetic association is recorded as CRADD[16].
  • syndromic intellectual disability's genetic association is recorded as TAOK1[17].
  • syndromic intellectual disability's genetic association is recorded as CTCF[18].
  • syndromic intellectual disability's genetic association is recorded as ASXL2[19].
  • syndromic intellectual disability's genetic association is recorded as HOXA1[20].
  • syndromic intellectual disability's genetic association is recorded as TRIO[21].
  • syndromic intellectual disability's genetic association is recorded as NSD2[22].
  • syndromic intellectual disability's genetic association is recorded as CDK13[23].
  • syndromic intellectual disability's genetic association is recorded as PUF60[24].
  • syndromic intellectual disability's genetic association is recorded as KAT6A[25].
  • syndromic intellectual disability's genetic association is recorded as PPP2R5D[26].

References

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

Direct Wikidata claims

  1. [2] . wikidata.org.
  2. [3] . wikidata.org.
  3. [4] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  4. [5] . wikidata.org.
  5. [6] . Disease Ontology. Retrieved . wikidata.org.
  6. [7] . wikidata.org.
  7. [8] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  8. [9] . X-linked spermine synthase gene (SMS) defect: the first polyamine deficiency syndrome. wikidata.org.
  9. [10] . UBE2A, which encodes a ubiquitin-conjugating enzyme, is mutated in a novel X-linked mental retardation syndrome. wikidata.org.
  10. [11] . Oligophrenin-1 encodes a rhoGAP protein involved in X-linked mental retardation. wikidata.org.
  11. [12] . ClinGen. Retrieved . search.clinicalgenome.org. Provenance: wikidata.org.
  12. [13] . ClinGen. Retrieved . search.clinicalgenome.org. Provenance: wikidata.org.
  13. [14] . ClinGen. Retrieved . search.clinicalgenome.org. Provenance: wikidata.org.
  14. [15] . ClinGen. Retrieved . search.clinicalgenome.org. Provenance: wikidata.org.
  15. [16] . ClinGen. Retrieved . search.clinicalgenome.org. Provenance: wikidata.org.
  16. [17] . ClinGen. Retrieved . search.clinicalgenome.org. Provenance: wikidata.org.
  17. [18] . ClinGen. Retrieved . search.clinicalgenome.org. Provenance: wikidata.org.
  18. [19] . ClinGen. Retrieved . search.clinicalgenome.org. Provenance: wikidata.org.
  19. [20] . ClinGen. Retrieved . search.clinicalgenome.org. Provenance: wikidata.org.
  20. [21] . ClinGen. Retrieved . search.clinicalgenome.org. Provenance: wikidata.org.
  21. [22] . ClinGen. Retrieved . search.clinicalgenome.org. Provenance: wikidata.org.
  22. [23] . ClinGen. Retrieved . search.clinicalgenome.org. Provenance: wikidata.org.
  23. [24] . ClinGen. Retrieved . search.clinicalgenome.org. Provenance: wikidata.org.
  24. [25] . ClinGen. Retrieved . search.clinicalgenome.org. Provenance: wikidata.org.
  25. [26] . ClinGen. Retrieved . search.clinicalgenome.org. Provenance: wikidata.org.

Class ancestry

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

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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). syndromic intellectual disability. Retrieved May 3, 2026, from https://4ort.xyz/entity/syndromic-intellectual-disability
MLA “syndromic intellectual disability.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/syndromic-intellectual-disability.
BibTeX @misc{4ortxyz_syndromic-intellectual-disability_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{syndromic intellectual disability}}, year = {2026}, url = {https://4ort.xyz/entity/syndromic-intellectual-disability}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): syndromic intellectual disability — https://4ort.xyz/entity/syndromic-intellectual-disability (retrieved 2026-05-03)

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