hereditary spastic paraplegia 7

hereditary spastic paraplegia that is characterized by slowly progressive onset, usually between 18-60 years of age, and generally more severe spasticity and has material basis in mutation in the SPG7 gene on chromosome 16q24
MedicalCondition developmental_defect_during_embryogenesis Q3363626
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hereditary spastic paraplegia 7

Summary

hereditary spastic paraplegia 7 is a developmental defect during embryogenesis[1]. It is known by 9 alternative names across languages and contexts.[2]

Key Facts

  • hereditary spastic paraplegia 7's instance of is recorded as developmental defect during embryogenesis[3].
  • hereditary spastic paraplegia 7's instance of is recorded as rare disease[4].
  • hereditary spastic paraplegia 7's instance of is recorded as class of disease[5].
  • hereditary spastic paraplegia 7 is a type of hereditary spastic paraplegia[6].
  • hereditary spastic paraplegia 7 is a type of nervous system heredodegenerative disease[7].
  • hereditary spastic paraplegia 7 is a type of pure or complex autosomal recessive spastic paraplegia[8].
  • hereditary spastic paraplegia 7 is a type of eye degenerative disease[9].
  • hereditary spastic paraplegia 7 is a type of cerebral degeneration[10].
  • hereditary spastic paraplegia 7 is a type of complex hereditary spastic paraplegia[11].
  • hereditary spastic paraplegia 7 is a type of combined oxidative phosphorylation deficiency[12].
  • hereditary spastic paraplegia 7 is a type of rare genetic developmental defect during embryogenesis[13].
  • hereditary spastic paraplegia 7 is a type of genetic movement disorder[14].
  • hereditary spastic paraplegia 7 is a type of syndromic hereditary optic neuropathy[15].
  • hereditary spastic paraplegia 7 is a type of autosomal recessive disease[16].
  • hereditary spastic paraplegia 7's NCI Thesaurus ID is recorded as C181657[17].
  • hereditary spastic paraplegia 7's health specialty is recorded as neurology[18].
  • hereditary spastic paraplegia 7's genetic association is recorded as SPG7[19].
  • hereditary spastic paraplegia 7's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110816[20].
  • hereditary spastic paraplegia 7's exact match is recorded as http://identifiers.org/doid/DOID:0110816[21].
  • hereditary spastic paraplegia 7's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_99013[22].
  • hereditary spastic paraplegia 7's on focus list of Wikimedia project is recorded as WikiProject Medicine[23].

Why It Matters

hereditary spastic paraplegia 7 is known by 9 alternative names across languages and contexts.[2]

References

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

Direct Wikidata claims

  1. [3] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . 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] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  7. [9] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  8. [10] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  9. [11] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  10. [12] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  11. [13] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  12. [14] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  13. [15] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  14. [16] ↑ . Disease Ontology. Retrieved . wikidata.org.
  15. [17] ↑ . wikidata.org.
  16. [18] ↑ . wikidata.org.
  17. [19] ↑ . Q905695. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  18. [20] ↑ . Disease Ontology. Retrieved . wikidata.org.
  19. [21] ↑ . Identifiers.org. registry.identifiers.org. Provenance: wikidata.org.
  20. [22] ↑ . wikidata.org.
  21. [23] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] ↑ . 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). hereditary spastic paraplegia 7. Retrieved October 10, 2026, from https://4ort.xyz/entity/hereditary-spastic-paraplegia-7
MLA “hereditary spastic paraplegia 7.” 4ort.xyz Knowledge Graph, 4ort.xyz, 10 Oct. 2026, https://4ort.xyz/entity/hereditary-spastic-paraplegia-7.
BibTeX @misc{4ortxyz_hereditary-spastic-paraplegia-7_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{hereditary spastic paraplegia 7}}, year = {2026}, url = {https://4ort.xyz/entity/hereditary-spastic-paraplegia-7}, note = {Accessed: 2026-10-10}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): hereditary spastic paraplegia 7 — https://4ort.xyz/entity/hereditary-spastic-paraplegia-7 (retrieved 2026-10-10)

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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. 14w ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Mondo id → MONDO_0011803
    Orphanet id → 99013
    Imported from → —
    Health specialty → neurology
    + 14 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/39742|batch #39742]]: subclass of disease, not instance"
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