hereditary spastic paraplegia 18

gene (8p11.2) encoding the protein, Erlin-2.

MedicalCondition rare_disease Q32142675

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Summary

hereditary spastic paraplegia 18 is a rare disease^[1]. It is known by 10 alternative names across languages and contexts.^[2]

Key Facts

Instance of: class of disease^[3]
Subclass of: hereditary spastic paraplegia^[4], autosomal recessive complex spastic paraplegia^[5], autosomal recessive disease^[6]
Health specialty: neurology^[7]
Genetic association: ERLIN2^[8]
Exact match: http://purl.obolibrary.org/obo/DOID_0110771^[9], http://identifiers.org/doid/DOID:0110771^[10], http://www.orpha.net/ORDO/Orphanet_209951^[11]
On focus list of Wikimedia project: WikiProject Medicine^[12]

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Quick Facts

Instance of rare disease, class of disease

Subclass of hereditary spastic paraplegia, autosomal recessive complex spastic paraplegia, autosomal recessive disease

Properties

Exact match purl.obolibrary.org, identifiers.org, www.orpha.net

Genetic association ERLIN2

Health specialty neurology

On focus list of wikimedia project WikiProject Medicine

External References (9)

Disease ontology id DOID:0110771

Gard rare disease id 4922

Icd-10-cm G11.4

Mesh descriptor id C567628

Mondo id MONDO_0012639

Omim id 611225

Orphanet id 209951

Umls cui C2749936

Uniprot disease id DI-03411

🏷️ Also known as

en autosomal recessive spastic paraplegia 18 en autosomal recessive spastic paraplegia type 18 en hereditary spastic paraplegia 18 en hereditary spastic paraplegia type 18 en IDMDC en intellectual disability, motor dysfunction and joint contractures en Intellectual Disability, Motor Dysfunction, and Joint Contractures en SPASTIC PARAPLEGIA 18, AUTOSOMAL RECESSIVE en SPASTIC PARAPLEGIA 18, AUTOSOMAL RECESSIVE; SPG18 en SPG18

References

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

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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). hereditary spastic paraplegia 18. Retrieved May 3, 2026, from https://4ort.xyz/entity/hereditary-spastic-paraplegia-18

MLA

“hereditary spastic paraplegia 18.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/hereditary-spastic-paraplegia-18.

BibTeX

@misc{4ortxyz_hereditary-spastic-paraplegia-18_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{hereditary spastic paraplegia 18}}, year = {2026}, url = {https://4ort.xyz/entity/hereditary-spastic-paraplegia-18}, note = {Accessed: 2026-05-03}}

LLM prompt

According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): hereditary spastic paraplegia 18 — https://4ort.xyz/entity/hereditary-spastic-paraplegia-18 (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/hereditary-spastic-paraplegia-18 · Last refreshed: May 3, 2026

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.

14w ago · JhealdBatch bot · 2026-07-05 view diff on Wikidata ↗

Mondo id → MONDO_0012639

Imported from → —

Umls cui → C2749936

Disease ontology id → DOID:0110771

+ 13 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)"

Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.

hereditary spastic paraplegia 18

Summary

Key Facts

References

Direct Wikidata claims

Class ancestry

Aggregate / graph-position facts

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