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Wikimedia neighborhood · Wikidata observation Observed Graph-projection

rare disease

disease that affects a small percentage of the population

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

Data and provenance

Provider: Wikidata · Entity ID: Q929833

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 (21)

← instance of← instance of← instance of← instance of← instance of← instance of← instance of← instance of← instance of← instance of← instance of← instance of← instance of← instance of← instance of← instance of← instance of← instance of← instance of← instance of← instance ofsyndactylyKabuki syndromemoya moya diseasemetabolic syndromeBarth syndromeprimary polydipsiaphaeochromocytomaX-linked adrenal hypo…Pelizaeus-Merzbacher …Marfan syndromeerythropoietic protop…Paget's disease of bo…focal segmental glome…osteitis fibrosa cyst…hypoparathyroidism-de…hereditary spastic pa…Apert syndromemultiple endocrine ne…Waardenburg's syndromethanatophoric dysplas…achromatopsiarare 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 (21)

  • ← instance of (P31)syndactylyObserved
    Relationship details

    Provider: Wikidata · Property: P31 · Direction: incoming · Entity ID: Q1360044

  • ← instance of (P31)Kabuki syndromeObserved
    Relationship details

    Provider: Wikidata · Property: P31 · Direction: incoming · Entity ID: Q1538227

  • ← instance of (P31)moya moya diseaseObserved
    Relationship details

    Provider: Wikidata · Property: P31 · Direction: incoming · Entity ID: Q1951267

  • ← instance of (P31)metabolic syndromeObserved
    Relationship details

    Provider: Wikidata · Property: P31 · Direction: incoming · Entity ID: Q657193

  • ← instance of (P31)Barth syndromeObserved
    Relationship details

    Provider: Wikidata · Property: P31 · Direction: incoming · Entity ID: Q928424

  • ← instance of (P31)primary polydipsiaObserved
    Relationship details

    Provider: Wikidata · Property: P31 · Direction: incoming · Entity ID: Q929963

  • ← instance of (P31)phaeochromocytomaObserved
    Relationship details

    Provider: Wikidata · Property: P31 · Direction: incoming · Entity ID: Q536269

  • ← instance of (P31)X-linked adrenal hypoplasia congenitaObserved
    Relationship details

    Provider: Wikidata · Property: P31 · Direction: incoming · Entity ID: Q3144300

  • ← instance of (P31)Pelizaeus-Merzbacher diseaseObserved
    Relationship details

    Provider: Wikidata · Property: P31 · Direction: incoming · Entity ID: Q1876206

  • ← instance of (P31)Marfan syndromeObserved
    Relationship details

    Provider: Wikidata · Property: P31 · Direction: incoming · Entity ID: Q208562

  • ← instance of (P31)erythropoietic protoporphyriaObserved
    Relationship details

    Provider: Wikidata · Property: P31 · Direction: incoming · Entity ID: Q1759600

  • ← instance of (P31)Paget's disease of boneObserved
    Relationship details

    Provider: Wikidata · Property: P31 · Direction: incoming · Entity ID: Q2035074

  • ← instance of (P31)focal segmental glomerulosclerosisObserved
    Relationship details

    Provider: Wikidata · Property: P31 · Direction: incoming · Entity ID: Q1435223

  • ← instance of (P31)osteitis fibrosa cysticaObserved
    Relationship details

    Provider: Wikidata · Property: P31 · Direction: incoming · Entity ID: Q799615

  • Relationship details

    Provider: Wikidata · Property: P31 · Direction: incoming · Entity ID: Q2027515

  • ← instance of (P31)hereditary spastic paraplegia 23Observed
    Relationship details

    Provider: Wikidata · Property: P31 · Direction: incoming · Entity ID: Q4664694

  • ← instance of (P31)Apert syndromeObserved
    Relationship details

    Provider: Wikidata · Property: P31 · Direction: incoming · Entity ID: Q618246

  • ← instance of (P31)multiple endocrine neoplasia type 2AObserved
    Relationship details

    Provider: Wikidata · Property: P31 · Direction: incoming · Entity ID: Q604075

  • ← instance of (P31)Waardenburg's syndromeObserved
    Relationship details

    Provider: Wikidata · Property: P31 · Direction: incoming · Entity ID: Q1151801

  • ← instance of (P31)thanatophoric dysplasiaObserved
    Relationship details

    Provider: Wikidata · Property: P31 · Direction: incoming · Entity ID: Q1787020

  • ← instance of (P31)achromatopsiaObserved
    Relationship details

    Provider: Wikidata · Property: P31 · Direction: incoming · Entity ID: Q432396

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