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erythropoietic protoporphyria

acute porphyria characterized by a deficiency in the enzyme ferrochelatase, leading to abnormally high levels of protoporphyrin in the tissue

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

Data and provenance

Provider: Wikidata · Entity ID: Q1759600

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 (17)

→ Relationship→ Relationship→ subclass of→ Relationship→ image→ instance of→ Relationship→ Commons category→ Relationship→ Relationship→ Relationship→ Relationship→ subclass of→ instance of→ Relationship→ subclass of← RelationshipALAS2http://www.orpha.net/…porphyria due to ALAD…FECHCutaneous histologica…rare diseasehttp://purl.obolibrar…Erythropoietic protop…endocrinologydermatologyWikiProject Medicinehttp://identifiers.or…porphyriatype of diseaseautosomal dominantErythropoietic porphy…FECHerythropoietic protoporphyr…
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.

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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 (5)

  • → subclass of (P279)porphyria due to ALAD deficiencyObserved
    Relationship details

    Provider: Wikidata · Property: P279 · Direction: outgoing · Entity ID: Q419897

  • → instance of (P31)rare diseaseObserved
    Relationship details

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

  • → subclass of (P279)porphyriaObserved
    Relationship details

    Provider: Wikidata · Property: P279 · Direction: outgoing · Entity ID: Q271759

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

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

  • → subclass of (P279)Erythropoietic porphyriaObserved
    Relationship details

    Provider: Wikidata · Property: P279 · Direction: outgoing · Entity ID: Q3908491

Other connections (10)

  • → Relationship name unavailable (P2293)ALAS2Observed
    Relationship details

    Provider: Wikidata · Property: P2293 · Direction: outgoing · Entity ID: Q17816607

  • → Relationship name unavailable (P2888)http://www.orpha.net/ORDO/Orphanet_79278Observed
    Relationship details

    Provider: Wikidata · Property: P2888 · Direction: outgoing

  • → Relationship name unavailable (P2293)FECHObserved
    Relationship details

    Provider: Wikidata · Property: P2293 · Direction: outgoing · Entity ID: Q14904856

  • → Relationship name unavailable (P2888)http://purl.obolibrary.org/obo/DOID_13270Observed
    Relationship details

    Provider: Wikidata · Property: P2888 · Direction: outgoing

  • → Relationship name unavailable (P1995)endocrinologyObserved
    Relationship details

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

  • → Relationship name unavailable (P1995)dermatologyObserved
    Relationship details

    Provider: Wikidata · Property: P1995 · Direction: outgoing · Entity ID: Q171171

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

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

  • → Relationship name unavailable (P2888)http://identifiers.org/doid/DOID:13270Observed
    Relationship details

    Provider: Wikidata · Property: P2888 · Direction: outgoing

  • → Relationship name unavailable (P1199)autosomal dominantObserved
    Relationship details

    Provider: Wikidata · Property: P1199 · Direction: outgoing · Entity ID: Q116406

  • ← Relationship name unavailable (P2293)FECHObserved
    Relationship details

    Provider: Wikidata · Property: P2293 · Direction: incoming · Entity ID: Q14904856

External identifiers (2)

  • → image (P18)Cutaneous histological features of EPP.jpgObserved
    Relationship details

    Provider: Wikidata · Property: P18 · Direction: outgoing

  • → Commons category (P373)Erythropoietic protoporphyriaObserved
    Relationship details

    Provider: Wikidata · Property: P373 · Direction: outgoing

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