Counterpedia · Subject

Wikidata observation

hereditary spastic paraplegia 23

hereditary spastic paraplegia that has material basis in variation in the chromosome region 1q24-q32

Also known as (10)

SPASTIC PARAPLEGIA 23; SPG23 · hereditary spastic paraplegia type 23 · spastic paraplegia 23 · spastic paraplegia type 23 · Spastic Paraparesis, Vitiligo, Premature Graying, Characteristic Facies · Autosomal recessive spastic paraplegia type 23 · spastic paraplegia with pigmentary abnormalities · SPG23 · Lison syndrome · Spastic paraparesis-vitiligo-premature graying-characteristic facies syndrome

Observations from Wikidata; separate from governed Counterpedia records. Sources, origins and what has been checked

At a glance

Selected recorded observations. Counterpedia has not independently verified them; inspect the statements for sources and alternative or historical context.

subclass of: phakomatosis
About this property
A broader class whose members include every member of this class. This is different from an individual being an instance of a class.
Wikidata property P279; Statement & references
instance of: type of disease
About this property
This names the relationship or attribute recorded by Wikidata. Any context shown beside it qualifies this particular statement.
Wikidata property P31; Statement & references

How these facts are selected

Up to eight distinct properties with readable names and values. One from each available category comes first, then remaining slots follow property category, property code and source order. This keeps names and family details from crowding out work, dates and geography. Media, external identifiers, unnamed targets and statements with incomplete qualifying context stay in the detailed list. The same rule applies to every subject. Context recorded by Wikidata appears beside each selected fact.

Relationships

Outgoing connections are statements about this subject. A connection is not evidence that another subject supports a claim.

subclass of (P279): phakomatosis
subclass of (P279): autosomal recessive diseaseRecorded context: Relationship name unavailable: named value unavailable in this release; has part(s): autosomal recessive complex spastic paraplegiaThis statement has context that cannot be fully shown here. An unresolved name or missing qualification can change how it should be understood.
Relationship name unavailable: DSTYK
subclass of (P279): hereditary spastic paraplegiaRecorded context: Relationship name unavailable: named value unavailable in this release; has part(s): autosomal recessive complex spastic paraplegiaThis statement has context that cannot be fully shown here. An unresolved name or missing qualification can change how it should be understood.
Relationship name unavailable: premature greying of hair
instance of (P31): type of disease
subclass of (P279): autosomal recessive complex spastic paraplegia
Relationship name unavailable: WikiProject Medicine
subclass of (P279): genetic diseaseRecorded context: Relationship name unavailable: named value unavailable in this release; has part(s): autosomal recessive complex spastic paraplegia; has part(s): autosomal recessive disease; has part(s): hereditary spastic paraplegiaThis statement has context that cannot be fully shown here. An unresolved name or missing qualification can change how it should be understood.
Relationship name unavailable: Adnan Abdallat
Relationship name unavailable: neurology
instance of (P31): rare disease

All projected connections & provider records

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hereditary spastic paraplegia 23

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Identity & relations

phakomatosis— subclass of (P279)stated relationship
autosomal recessive disease— subclass of (P279)stated relationship
hereditary spastic paraplegia— subclass of (P279)stated relationship
type of disease— instance of (P31)stated relationship
autosomal recessive complex spastic paraplegia— subclass of (P279)stated relationship
genetic disease— subclass of (P279)stated relationship
rare disease— instance of (P31)stated relationship

Other connections

DSTYK— P2293stated relationship
premature greying of hair— P7500stated relationship
WikiProject Medicine— P5008stated relationship
Adnan Abdallat— P61stated relationship
neurology— P1995stated relationship

The original records this observation was assembled from, off Counterpedia.

Wikidata: Q4664694 ↗

Keep exploring the surrounding neighborhood.

Explore the hereditary spastic paraplegia 23 neighborhood

Assembled from entry read model wikimedia_observation:Q4664694, public release sha256:f33228901a35b0683356002a46df9ceb11f399d05f17abb5c7c78256cbf38ba7. This view is served from published release bytes.

Explore incoming and outgoing relationships →

External identifiers (9)

Identifier lookup links, separate from statement references.

P4317: 336
P492: 270750
P486: C536859
P2892: C0796019
P5270: MONDO_0010046
P11430: DI-04976
P4229: G11.4
P699: DOID:0110774
P1550: 101003

Sources and origins

Structured observations: Statements in this view were observed in Wikidata. Their source identifiers and carried history remain available for inspection.
Cited references: Works, URLs and identifiers attached to particular statements. A cited locator is not an independently established support finding. Inspect statement references
Retained evidence: This view carries observation data. It does not supply independently captured copies of the cited documents or establish their custody. Discovering a reference does not register a governed Source Record.
Checks: No completed Check is associated with these statements in this view. Check execution is currently unavailable.

These observations are not governed Counterpedia claims. The origin of an observation can differ from the author or publisher of its cited source.

Documentary coverage

Documentary identifiers

No source identifiers recorded

Identifiers Counterpedia can route

No lookup route known

Reference-route hints

Reference route hint recorded

“Routable” means Counterpedia knows an approved provider capability that can investigate the identifier. It does not mean the source has been captured or checked.

Validation state

1. In Wikidata
No source identifiers recorded.
2. Lookup route
No source identifiers recorded.
3. Lookup result
No lookup recorded for this page.
4. Saved copy
No saved copy for this page.
5. Fixed version
No fixed source version for this page.
6. Check result
Not checked.

These stages describe what this page can show from governed subject-scoped records. A lookup route does not mean a source was found; a lookup result does not mean bytes were saved; and a saved copy does not mean a fixed source version or a Check result exists.

Research frontier

Ready to investigate

None of the recorded identifier routes is marked routable.

Still unresolved

9 identifier routes and 17 reference hints remain research inputs rather than governed evidence.

Authority boundary

What this page establishes

It establishes what the retained Wikimedia observation contains and what investigation paths Counterpedia can describe from that material.

What it does not establish

A Wikidata statement is not automatically Counterpedia evidence.
A routable identifier is not a captured source.
A captured representation is not automatically a fixed source version.
A fixed source version is not automatically a Check result.
Graph proximity and reference counts are not support or corroboration.
A provider observation and candidate locator do not establish source bytes or support.

Presentation contract

Stage template: counterpedia.reader.profile.v1
Counterpedia composition: counterpedia.product.subject.profile.v1

Statements & recorded references

Open a statement to see the references attached to it. Context can limit when, where or how a statement applies. Recorded source URLs, identifier resolvers and source works describe where Wikidata points; none establishes source support or a completed Check.

Check execution is unavailable in this preview. Exact recorded locators remain available to inspect and open.

subclass of: phakomatosisReference count not carried
Observation origin: Wikidata. References below are citations attached to this statement, not independently captured evidence.
About this property
A broader class whose members include every member of this class. This is different from an individual being an instance of a class.
Wikidata property P279
No exact source locator is carried for this statement in this view.
Statement identity, reference hashes and carried detail
```
{
  "predicate": "P279",
  "targetRef": "Q748376",
  "targetLabel": "phakomatosis"
}
```

subclass of: autosomal recessive disease1 recorded referenceRecorded context: Relationship name unavailable: named value unavailable in this release; has part(s): autosomal recessive complex spastic paraplegiaThis statement has context that cannot be fully shown here. An unresolved name or missing qualification can change how it should be understood.

Observation origin: Wikidata. References below are citations attached to this statement, not independently captured evidence.

About this property

A broader class whose members include every member of this class. This is different from an individual being an instance of a class.

Wikidata property P279

No exact source locator is carried for this statement in this view.

Qualifiers

Relationship name unavailable: named value unavailable in this release

has part(s): autosomal recessive complex spastic paraplegia

Statement identity, reference hashes and carried detail

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Relationship name unavailable: DSTYK2 recorded references
Observation origin: Wikidata. References below are citations attached to this statement, not independently captured evidence.
About this property
The readable name for this property is unavailable here. Its code and exact recorded value are preserved; the code alone does not explain the relationship.
Wikidata property P2293
No exact source locator is carried for this statement in this view.
Statement identity, reference hashes and carried detail
```
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```
Relationship name unavailable: http://purl.obolibrary.org/obo/DOID_01107741 recorded reference
Observation origin: Wikidata. References below are citations attached to this statement, not independently captured evidence.
About this property
The readable name for this property is unavailable here. Its code and exact recorded value are preserved; the code alone does not explain the relationship.
Wikidata property P2888
No exact source locator is carried for this statement in this view.
Statement identity, reference hashes and carried detail
```
{
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}
```

subclass of: hereditary spastic paraplegia1 recorded referenceRecorded context: Relationship name unavailable: named value unavailable in this release; has part(s): autosomal recessive complex spastic paraplegiaThis statement has context that cannot be fully shown here. An unresolved name or missing qualification can change how it should be understood.

Observation origin: Wikidata. References below are citations attached to this statement, not independently captured evidence.

About this property

A broader class whose members include every member of this class. This is different from an individual being an instance of a class.

Wikidata property P279

No exact source locator is carried for this statement in this view.

Qualifiers

Relationship name unavailable: named value unavailable in this release

has part(s): autosomal recessive complex spastic paraplegia

Statement identity, reference hashes and carried detail

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}

Relationship name unavailable: premature greying of hair1 recorded reference
Observation origin: Wikidata. References below are citations attached to this statement, not independently captured evidence.
About this property
The readable name for this property is unavailable here. Its code and exact recorded value are preserved; the code alone does not explain the relationship.
Wikidata property P7500
No exact source locator is carried for this statement in this view.
Statement identity, reference hashes and carried detail
```
{
  "predicate": "P7500",
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```
instance of: type of diseaseReference count not carried
Observation origin: Wikidata. References below are citations attached to this statement, not independently captured evidence.
About this property
This names the relationship or attribute recorded by Wikidata. Any context shown beside it qualifies this particular statement.
Wikidata property P31
No exact source locator is carried for this statement in this view.
Statement identity, reference hashes and carried detail
```
{
  "predicate": "P31",
  "targetRef": "Q112193867",
  "targetLabel": "type of disease"
}
```
Relationship name unavailable: http://identifiers.org/doid/DOID:01107741 recorded reference
Observation origin: Wikidata. References below are citations attached to this statement, not independently captured evidence.
About this property
The readable name for this property is unavailable here. Its code and exact recorded value are preserved; the code alone does not explain the relationship.
Wikidata property P2888
No exact source locator is carried for this statement in this view.
Statement identity, reference hashes and carried detail
```
{
  "predicate": "P2888",
  "literalValue": "http://identifiers.org/doid/DOID:0110774",
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```
subclass of: autosomal recessive complex spastic paraplegia1 recorded reference
Observation origin: Wikidata. References below are citations attached to this statement, not independently captured evidence.
About this property
A broader class whose members include every member of this class. This is different from an individual being an instance of a class.
Wikidata property P279
No exact source locator is carried for this statement in this view.
Statement identity, reference hashes and carried detail
```
{
  "predicate": "P279",
  "targetRef": "Q55345926",
  "targetLabel": "autosomal recessive complex spastic paraplegia",
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    "propertyPidSummaryTruncated": false,
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  }
}
```
Relationship name unavailable: WikiProject MedicineReference count not carried
Observation origin: Wikidata. References below are citations attached to this statement, not independently captured evidence.
About this property
The readable name for this property is unavailable here. Its code and exact recorded value are preserved; the code alone does not explain the relationship.
Wikidata property P5008
No exact source locator is carried for this statement in this view.
Statement identity, reference hashes and carried detail
```
{
  "predicate": "P5008",
  "targetRef": "Q4099686",
  "targetLabel": "WikiProject Medicine"
}
```

subclass of: genetic disease1 recorded referenceRecorded context: Relationship name unavailable: named value unavailable in this release; has part(s): autosomal recessive complex spastic paraplegia; has part(s): autosomal recessive disease; has part(s): hereditary spastic paraplegiaThis statement has context that cannot be fully shown here. An unresolved name or missing qualification can change how it should be understood.

Observation origin: Wikidata. References below are citations attached to this statement, not independently captured evidence.

About this property

A broader class whose members include every member of this class. This is different from an individual being an instance of a class.

Wikidata property P279

No exact source locator is carried for this statement in this view.

Qualifiers

Relationship name unavailable: named value unavailable in this release

has part(s): autosomal recessive complex spastic paraplegia

has part(s): autosomal recessive disease

has part(s): hereditary spastic paraplegia

Statement identity, reference hashes and carried detail

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Relationship name unavailable: Adnan AbdallatReference count not carried
Observation origin: Wikidata. References below are citations attached to this statement, not independently captured evidence.
About this property
The readable name for this property is unavailable here. Its code and exact recorded value are preserved; the code alone does not explain the relationship.
Wikidata property P61
No exact source locator is carried for this statement in this view.
Statement identity, reference hashes and carried detail
```
{
  "predicate": "P61",
  "targetRef": "Q4683852",
  "targetLabel": "Adnan Abdallat"
}
```
Relationship name unavailable: neurologyReference count not carried
Observation origin: Wikidata. References below are citations attached to this statement, not independently captured evidence.
About this property
The readable name for this property is unavailable here. Its code and exact recorded value are preserved; the code alone does not explain the relationship.
Wikidata property P1995
No exact source locator is carried for this statement in this view.
Statement identity, reference hashes and carried detail
```
{
  "predicate": "P1995",
  "targetRef": "Q83042",
  "targetLabel": "neurology"
}
```
instance of: rare diseaseReference count not carried
Observation origin: Wikidata. References below are citations attached to this statement, not independently captured evidence.
About this property
This names the relationship or attribute recorded by Wikidata. Any context shown beside it qualifies this particular statement.
Wikidata property P31
No exact source locator is carried for this statement in this view.
Statement identity, reference hashes and carried detail
```
{
  "predicate": "P31",
  "targetRef": "Q929833",
  "targetLabel": "rare disease"
}
```
Relationship name unavailable: http://www.orpha.net/ORDO/Orphanet_101003Reference count not carried
Observation origin: Wikidata. References below are citations attached to this statement, not independently captured evidence.
About this property
The readable name for this property is unavailable here. Its code and exact recorded value are preserved; the code alone does not explain the relationship.
Wikidata property P2888
No exact source locator is carried for this statement in this view.
Statement identity, reference hashes and carried detail
```
{
  "predicate": "P2888",
  "literalValue": "http://www.orpha.net/ORDO/Orphanet_101003"
}
```

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Data and provenance

Wikidata entity IDs are external identifiers, not Counterpedia canonical subject identities. Rendering this page does not mint a governed identity. Release identities and artifact hashes identify the data used for this view; none establishes verification.

Provenance rows: 36
Acquisition repository: thelaplage/counterpedia-acquisition
Acquisition revision: e6add6a4d8e1668a9ac486407e52974724563ce1, 891f24c5cca64aa69b1dc1b2150e991b940171b0
Provider identity · Observation origin: Wikidata · External entity ID: Q4664694 on Wikidata ↗
Served release: sha256:f33228901a35b0683356002a46df9ceb11f399d05f17abb5c7c78256cbf38ba7

No exact claim–source–Check association has been supplied to this page. Recorded references do not establish verification.

graph_membership != truth
graph_edge != support
repeated_identifier != independent_corroboration
projection != admission
Serving a published subset: joined entities + 1-hop neighborhood of 35,994 exact Wikipedia–Wikidata title matches.

Carried provenance rows

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Classification identities

[
  {
    "classQid": "Q112193867",
    "label": "type of disease",
    "href": "/browse/types/Q112193867"
  },
  {
    "classQid": "Q929833",
    "label": "rare disease",
    "href": "/browse/types/Q929833"
  }
]

Wikidata content CC0; Wikipedia titles CC BY-SA — attribution.