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Pelizaeus-Merzbacher disease

hypomyelinating leukodystrophy characterized by impaired myelin formation, nystagmus, spastic quadriplegia, ataxia, and developmental delay that has material basis in mutation in the PLP1 gene on chromosome Xq22

Provider: Wikidata. These recorded connections are observations, not Counterpedia claims. They do not establish source support.

Data and provenance

Provider: Wikidata · Entity ID: Q1876206

Release: sha256:f33228901a35b0683356002a46df9ceb11f399d05f17abb5c7c78256cbf38ba7

Graph membership is not truth. Each relation below is an observed typed edge the local Wikimedia graph bundle already materialized — not a corroborated, verified, or admitted claim. Bounded to 40 relations via an offset-index lookup (offset_index_binary_search), never a full scan of the bundle.Serving a published subset: joined entities + 1-hop neighborhood of 35,994 exact Wikipedia–Wikidata title matches. A subject that is not itself in that subset carries only the relations the subset recorded for it, so a small count here is the published scope and not a complete relationship inventory.
Development requests are not available on this deployment. The observed entity and its graph links remain readable.

1-hop relations (16)

→ Relationship→ subclass of→ instance of→ named after→ subclass of→ instance of→ Relationship→ named after→ Relationship→ subclass of→ Relationship→ Relationship→ subclass of→ Relationship→ Relationship← Relationshiphttp://identifiers.or…nervous system heredo…type of diseaseLudwig MerzbacherX-linked recessive di…rare diseaseWikiProject MedicineFriedrich Christoph P…http://purl.obolibrar…eye degenerative dise…neurologyhttp://purl.obolibrar…hypomyelinating leuko…PLP1http://www.orpha.net/…PLP1Pelizaeus-Merzbacher disease
Observed adjacency only. Each spoke is a typed edge already materialized in the graph, labeled by its recorded predicate — graph proximity is not support, corroboration, or admission. The links below are the accessible, no-JavaScript path to the same neighbors.

Follow a connection

Grouped by a fixed presentation taxonomy for legibility only. The grouping asserts no rank, truth, support, or standing — every observed edge is carried, none reordered by importance.

Identity & relations (6)

  • → subclass of (P279)nervous system heredodegenerative diseaseObserved
    Relationship details

    Provider: Wikidata · Property: P279 · Direction: outgoing · Entity ID: Q19001236

  • → instance of (P31)type of diseaseObserved
    Relationship details

    Provider: Wikidata · Property: P31 · Direction: outgoing · Entity ID: Q112193867

  • → subclass of (P279)X-linked recessive diseaseObserved
    Relationship details

    Provider: Wikidata · Property: P279 · Direction: outgoing · Entity ID: Q55010090

  • → instance of (P31)rare diseaseObserved
    Relationship details

    Provider: Wikidata · Property: P31 · Direction: outgoing · Entity ID: Q929833

  • → subclass of (P279)eye degenerative diseaseObserved
    Relationship details

    Provider: Wikidata · Property: P279 · Direction: outgoing · Entity ID: Q18558225

  • → subclass of (P279)hypomyelinating leukodystrophyObserved
    Relationship details

    Provider: Wikidata · Property: P279 · Direction: outgoing · Entity ID: Q28065591

Other connections (10)

  • → Relationship name unavailable (P2888)http://identifiers.org/doid/DOID:3210Observed
    Relationship details

    Provider: Wikidata · Property: P2888 · Direction: outgoing

  • → named after (P138)Ludwig MerzbacherObserved
    Relationship details

    Provider: Wikidata · Property: P138 · Direction: outgoing · Entity ID: Q92286

  • → Relationship name unavailable (P5008)WikiProject MedicineObserved
    Relationship details

    Provider: Wikidata · Property: P5008 · Direction: outgoing · Entity ID: Q4099686

  • → named after (P138)Friedrich Christoph PelizaeusObserved
    Relationship details

    Provider: Wikidata · Property: P138 · Direction: outgoing · Entity ID: Q97219

  • → Relationship name unavailable (P2888)http://purl.obolibrary.org/obo/HP_0003269Observed
    Relationship details

    Provider: Wikidata · Property: P2888 · Direction: outgoing

  • → Relationship name unavailable (P1995)neurologyObserved
    Relationship details

    Provider: Wikidata · Property: P1995 · Direction: outgoing · Entity ID: Q83042

  • → Relationship name unavailable (P2888)http://purl.obolibrary.org/obo/DOID_3210Observed
    Relationship details

    Provider: Wikidata · Property: P2888 · Direction: outgoing

  • → Relationship name unavailable (P2293)PLP1Observed
    Relationship details

    Provider: Wikidata · Property: P2293 · Direction: outgoing · Entity ID: Q14912011

  • → Relationship name unavailable (P2888)http://www.orpha.net/ORDO/Orphanet_702Observed
    Relationship details

    Provider: Wikidata · Property: P2888 · Direction: outgoing

  • ← Relationship name unavailable (P2293)PLP1Observed
    Relationship details

    Provider: Wikidata · Property: P2293 · Direction: incoming · Entity ID: Q14912011

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