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spastic quadriplegia

type of spastic cerebral palsy characterized by increased muscle tone of all four extremities
Class type of: spastic cerebral palsy, nervous system heredodegenerative disease Q3985306

Facts

12 properties
Instance of
rare disease, class of disease[2]
Subclass of
spastic cerebral palsy, nervous system heredodegenerative disease[3][4]
Age of onset
infantile onset, neonatal onset[17][18]
Drug or therapy used for treatment
dantrolene, (RS)-baclofen[11][12]
Genetic association
KANK1, ADD3, GAD1, HPDL[13][14][15][16]
Health specialty
neurology[10]
ICD-9-CM
343.2, 344.09[7][8]
NCI Thesaurus ID
C116904[9]
On focus list of Wikimedia project
WikiProject Medicine[19]
P14914
D210141[20]
Prevalence
+0.000001[6]
Symptoms and signs
quadrispasticity[5]
🏷️ Also known as
en tetraplegic infantile cerebral palsy en Inherited congenital spastic quadriplegia en Inherited congenital spastic tetraplegia en quadriplegic infantile cerebral palsy en spastic quadriplegia en spastic quadriplegic cerebral palsy ar شلل رباعي تشنجي es cuadriplejia espástica es tetraplejia espástica fr quadriplégie spastique it Tetraparesi spastica it tetraplegia spastica ja 痙性四肢麻痺
🔖 Identifiers · 16
OpenAlex ID
C2777827993
Disease Ontology ID
DOID:10970
Exact match
purl.obolibrary.org, identifiers.org, www.orpha.net
Human Phenotype Ontology ID
HP:0002510
ICD-10 ID
G80.0
ICD-10-CM
G11.4
ICD-11 ID (Foundation)
1155284708, 1591776568
ICD-11 ID (MMS)
8D20.10
KEGG ID
H01097
Medical Dictionary for Regulatory Activities ID
10021744
Microsoft Academic ID (discontinued)
2777827993, 2908678573
Mondo ID
MONDO_0016215
Show all 16 identifiers +4
OMIM ID
603513, 612900
Orphanet ID
210141
Quora topic ID
Spastic-Quadriplegia
UMLS CUI
C0426970, C0154697

Report an error or request removal Lineage (PROV-JSON)

🔗 Connections
Genetic association 3
ADD3, GAD1, KANK1
Drug or therapy used for treatment 2
(RS)-baclofen, dantrolene
← Medical condition 2
Frank Williams, Philippe Streiff
Health specialty 1
neurology
Instance of 1
rare disease
On focus list of Wikimedia project 1
WikiProject Medicine
Subclass of 1
spastic cerebral palsy
← Different from 1
monoplegia
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Summary

spastic quadriplegia is a rare disease[1].

Related Entities

Frank Williams neurology

References

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

Direct Wikidata claims

  1. [2] ↑ . wikidata.org.
  2. [3] ↑ . Disease Ontology. Retrieved . wikidata.org.
  3. [4] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  4. [5] ↑ . wikidata.org.
  5. [6] ↑ . Retrieved . wikidata.org.
  6. [7] ↑ . Disease Ontology. Retrieved . wikidata.org.
  7. [8] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  8. [9] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  9. [10] ↑ . wikidata.org.
  10. [11] ↑ . NDF-RT. Retrieved . wikidata.org.
  11. [12] ↑ . NDF-RT. Retrieved . wikidata.org.
  12. [13] ↑ . Deletion of the ANKRD15 gene at 9p24.3 causes parent-of-origin-dependent inheritance of familial cerebral palsy. wikidata.org.
  13. [14] ↑ . Mutations in γ adducin are associated with inherited cerebral palsy.. wikidata.org.
  14. [15] ↑ . Homozygosity for a missense mutation in the 67 kDa isoform of glutamate decarboxylase in a family with autosomal recessive spastic cerebral palsy: parallels with Stiff-Person Syndrome and other movement disorders. wikidata.org.
  15. [16] ↑ . Retrieved . wikidata.org.
  16. [17] ↑ . Retrieved . wikidata.org.
  17. [18] ↑ . Retrieved . wikidata.org.
  18. [19] ↑ . wikidata.org.
  19. [20] ↑ . 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). spastic quadriplegia. Retrieved November 6, 2026, from https://4ort.xyz/entity/spastic-quadriplegia
MLA “spastic quadriplegia.” 4ort.xyz Knowledge Graph, 4ort.xyz, 6 Nov. 2026, https://4ort.xyz/entity/spastic-quadriplegia.
BibTeX @misc{4ortxyz_spastic-quadriplegia_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{spastic quadriplegia}}, year = {2026}, url = {https://4ort.xyz/entity/spastic-quadriplegia}, note = {Accessed: 2026-11-06}}
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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. 13d ago · ACorrêa (WMB) · 2026-10-23 view diff on Wikidata ↗
    Genetic association → KANK1, ADD3, GAD1 +1
    Prevalence → {'amount': '+0.000001'}
    Age of onset → infantile onset, neonatal onset
    P14914 → D210141
    + 1 other property edited (see Wikidata diff for full list)
    "/* wbeditentity-update-languages-and-other-short:0||pt, pt-br */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/61469|batch #61469]]: Raras.org data import"
  2. 14d ago · ACorrêa (WMB) · 2026-10-23 view diff on Wikidata ↗
    Instance of → rare disease, class of disease
    On focus list of Wikimedia project → WikiProject Medicine
    Wikipedia languages → ['ar', 'en', 'es', 'it', 'mk']
    Subclass of → —
    + 8 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/61242|batch #61242]]: HPO ID through mesh or umls"
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