CounterpediaExplore knowledge. Follow the sources.

Wikimedia neighborhood · Wikidata observation Observed Graph-projection

Barth syndrome

lipid metabolism disorder that has material basis in X-linked inheritance of the tafazzin gene and is characterized by decreased production of an enzyme required to produce cardiolipin

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

Data and provenance

Provider: Wikidata · Entity ID: Q928424

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 (40+)

→ Relationship→ Relationship→ subclass of→ Relationship→ Relationship→ Relationship→ Relationship→ Relationship→ Relationship→ Commons category→ Relationship→ subclass of→ Relationship→ Relationship→ Relationship→ instance of→ Relationship→ Relationship→ Relationship→ Relationship→ Relationship→ subclass of→ Relationship→ Relationship→ Relationship→ Relationship→ Relationship→ subclass of→ Relationship→ Relationship→ Relationship→ Relationship→ subclass of→ Relationship→ subclass of→ Relationship→ image→ Relationship→ Relationship← RelationshipBroad foreheadhttp://purl.obolibrar…lipid metabolism diso…lipoatrophypalmoplantar keratosisAbnormal mitochondria…muscular diseaseheart failureMacrotiaBarth syndromeclubfootmitochondrial myopathyX-linked recessiveendocrinology3-methylglutaconic ac…rare diseaseTAFAZZINhttp://www.orpha.net/…Round faceWikiProject Medicinesensorineural hearing…disorder of phospholi…agranulocytosisfatigueorganic acidemiaGrowth delayfailure to thriveX-linked recessive di…Full cheeksRecurrent infections …dilated cardiomyopathySkeletal myopathyconstitutional neutro…Abnormality of neutro…developmental defect …gait abnormalityCardiolipin.svghypertrophic cardiomy…heart arrhythmiaTAFAZZINBarth syndrome
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 (7)

Other connections (31)

  • → Relationship name unavailable (P6532)Broad foreheadObserved
    Relationship details

    Provider: Wikidata · Property: P6532 · Direction: outgoing · Entity ID: Q110938526

  • → Relationship name unavailable (P2888)http://purl.obolibrary.org/obo/DOID_0050476Observed
    Relationship details

    Provider: Wikidata · Property: P2888 · Direction: outgoing

  • → Relationship name unavailable (P780)lipoatrophyObserved
    Relationship details

    Provider: Wikidata · Property: P780 · Direction: outgoing · Entity ID: Q3500973

  • → Relationship name unavailable (P780)palmoplantar keratosisObserved
    Relationship details

    Provider: Wikidata · Property: P780 · Direction: outgoing · Entity ID: Q7128426

  • → Relationship name unavailable (P6532)Abnormal mitochondrial morphologyObserved
    Relationship details

    Provider: Wikidata · Property: P6532 · Direction: outgoing · Entity ID: Q110938521

  • → Relationship name unavailable (P780)muscular diseaseObserved
    Relationship details

    Provider: Wikidata · Property: P780 · Direction: outgoing · Entity ID: Q692536

  • → Relationship name unavailable (P780)heart failureObserved
    Relationship details

    Provider: Wikidata · Property: P780 · Direction: outgoing · Entity ID: Q181754

  • → Relationship name unavailable (P780)MacrotiaObserved
    Relationship details

    Provider: Wikidata · Property: P780 · Direction: outgoing · Entity ID: Q3842198

  • → Relationship name unavailable (P780)clubfootObserved
    Relationship details

    Provider: Wikidata · Property: P780 · Direction: outgoing · Entity ID: Q1162164

  • → Relationship name unavailable (P780)X-linked recessiveObserved
    Relationship details

    Provider: Wikidata · Property: P780 · Direction: outgoing · Entity ID: Q1988987

  • → Relationship name unavailable (P1995)endocrinologyObserved
    Relationship details

    Provider: Wikidata · Property: P1995 · Direction: outgoing · Entity ID: Q162606

  • → Relationship name unavailable (P780)3-methylglutaconic aciduriaObserved
    Relationship details

    Provider: Wikidata · Property: P780 · Direction: outgoing · Entity ID: Q3598794

  • → Relationship name unavailable (P2293)TAFAZZINObserved
    Relationship details

    Provider: Wikidata · Property: P2293 · Direction: outgoing · Entity ID: Q14881093

  • → Relationship name unavailable (P2888)http://www.orpha.net/ORDO/Orphanet_111Observed
    Relationship details

    Provider: Wikidata · Property: P2888 · Direction: outgoing

  • → Relationship name unavailable (P6532)Round faceObserved
    Relationship details

    Provider: Wikidata · Property: P6532 · Direction: outgoing · Entity ID: Q110938499

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

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

  • → Relationship name unavailable (P780)sensorineural hearing lossObserved
    Relationship details

    Provider: Wikidata · Property: P780 · Direction: outgoing · Entity ID: Q928697

  • → Relationship name unavailable (P780)agranulocytosisObserved
    Relationship details

    Provider: Wikidata · Property: P780 · Direction: outgoing · Entity ID: Q396013

  • → Relationship name unavailable (P780)fatigueObserved
    Relationship details

    Provider: Wikidata · Property: P780 · Direction: outgoing · Entity ID: Q9690

  • → Relationship name unavailable (P780)organic acidemiaObserved
    Relationship details

    Provider: Wikidata · Property: P780 · Direction: outgoing · Entity ID: Q1547640

  • → Relationship name unavailable (P6532)Growth delayObserved
    Relationship details

    Provider: Wikidata · Property: P6532 · Direction: outgoing · Entity ID: Q110938514

  • → Relationship name unavailable (P780)failure to thriveObserved
    Relationship details

    Provider: Wikidata · Property: P780 · Direction: outgoing · Entity ID: Q1497481

  • → Relationship name unavailable (P6532)Full cheeksObserved
    Relationship details

    Provider: Wikidata · Property: P6532 · Direction: outgoing · Entity ID: Q110938491

  • → Relationship name unavailable (P6532)Recurrent infections in infancy and early childhoodObserved
    Relationship details

    Provider: Wikidata · Property: P6532 · Direction: outgoing · Entity ID: Q110938494

  • → Relationship name unavailable (P780)dilated cardiomyopathyObserved
    Relationship details

    Provider: Wikidata · Property: P780 · Direction: outgoing · Entity ID: Q283656

  • → Relationship name unavailable (P6532)Skeletal myopathyObserved
    Relationship details

    Provider: Wikidata · Property: P6532 · Direction: outgoing · Entity ID: Q110938505

  • → Relationship name unavailable (P6532)Abnormality of neutrophilsObserved
    Relationship details

    Provider: Wikidata · Property: P6532 · Direction: outgoing · Entity ID: Q110938519

  • → Relationship name unavailable (P780)gait abnormalityObserved
    Relationship details

    Provider: Wikidata · Property: P780 · Direction: outgoing · Entity ID: Q827017

  • → Relationship name unavailable (P780)hypertrophic cardiomyopathyObserved
    Relationship details

    Provider: Wikidata · Property: P780 · Direction: outgoing · Entity ID: Q1364270

  • → Relationship name unavailable (P780)heart arrhythmiaObserved
    Relationship details

    Provider: Wikidata · Property: P780 · Direction: outgoing · Entity ID: Q189331

  • ← Relationship name unavailable (P2293)TAFAZZINObserved
    Relationship details

    Provider: Wikidata · Property: P2293 · Direction: incoming · Entity ID: Q14881093

External identifiers (2)

  • → Commons category (P373)Barth syndromeObserved
    Relationship details

    Provider: Wikidata · Property: P373 · Direction: outgoing

  • → image (P18)Cardiolipin.svgObserved
    Relationship details

    Provider: Wikidata · Property: P18 · Direction: outgoing

More relations exist beyond this bounded panel's cap of 40. This panel intentionally shows a small neighborhood, not the full graph.

Return to entry