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Sialidosis type 1

lysosomal storage disease
MedicalCondition rare_disease Q7506658
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Sialidosis type 1

Summary

Sialidosis type 1 is a rare disease[1].

Key Facts

  • Sialidosis type 1's instance of is recorded as rare disease[2].
  • Sialidosis type 1's instance of is recorded as class of disease[3].
  • Sialidosis type 1 is a type of glycoproteinosis[4].
  • Sialidosis type 1 is a type of sialidosis[5].
  • Sialidosis type 1's health specialty is recorded as endocrinology[6].
  • Sialidosis type 1's genetic association is recorded as NEU1[7].
  • Sialidosis type 1's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_812[8].

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] ↑ . wikidata.org.
  4. [5] ↑ . wikidata.org.
  5. [6] ↑ . wikidata.org.
  6. [7] ↑ . Open Targets Platform. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  7. [8] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. 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). Sialidosis type 1. Retrieved May 3, 2026, from https://4ort.xyz/entity/sialidosis-type-1
MLA “Sialidosis type 1.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/sialidosis-type-1.
BibTeX @misc{4ortxyz_sialidosis-type-1_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Sialidosis type 1}}, year = {2026}, url = {https://4ort.xyz/entity/sialidosis-type-1}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Sialidosis type 1 — https://4ort.xyz/entity/sialidosis-type-1 (retrieved 2026-05-03)

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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. 17d ago · JhealdBatch bot · 2026-07-05 view diff on Wikidata ↗
    Emedicine id → 948704
    Icd-11 id (foundation) → 1154773192
    Gard rare disease id → 7639
    Health specialty → endocrinology
    + 18 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/39953|batch #39953]]: deprecate redundant disease superclasses (2)"
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