Wikimedia neighborhood · Wikidata observation Observed Graph-projection

Aicardi syndrome

syndrome that is characterized by absence or underdeveloped tissue connecting the left and right halves of the brain, infantile spasms and chorioretinal lacunae, which are defects in the light-sensitive tissue at the back of the eye

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

Data and provenance

Provider: Wikidata · Entity ID: Q403463

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 (22)

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 (11)

→ subclass of (P279)syndromeObserved
Relationship details
Provider: Wikidata · Property: P279 · Direction: outgoing · Entity ID: Q179630
→ instance of (P31)symptom or signObserved
Relationship details
Provider: Wikidata · Property: P31 · Direction: outgoing · Entity ID: Q112965645
→ subclass of (P279)developmental defect during embryogenesisObserved
Relationship details
Provider: Wikidata · Property: P279 · Direction: outgoing · Entity ID: Q55788864
→ instance of (P31)type of diseaseObserved
Relationship details
Provider: Wikidata · Property: P31 · Direction: outgoing · Entity ID: Q112193867
→ subclass of (P279)nervous system anomaly with eye involvementObserved
Relationship details
Provider: Wikidata · Property: P279 · Direction: outgoing · Entity ID: Q55789255
→ subclass of (P279)syndromic developmental defect of the eyeObserved
Relationship details
Provider: Wikidata · Property: P279 · Direction: outgoing · Entity ID: Q55785336
→ instance of (P31)designated intractable/rare diseaseObserved
Relationship details
Provider: Wikidata · Property: P31 · Direction: outgoing · Entity ID: Q42303753
→ subclass of (P279)cerebral malformation with epilepsyObserved
Relationship details
Provider: Wikidata · Property: P279 · Direction: outgoing · Entity ID: Q55785630
→ subclass of (P279)genetic syndrome with corpus callosum agenesis/dysgenesis as a major featureObserved
Relationship details
Provider: Wikidata · Property: P279 · Direction: outgoing · Entity ID: Q55786837
→ subclass of (P279)X-linked intellectual disabilityObserved
Relationship details
Provider: Wikidata · Property: P279 · Direction: outgoing · Entity ID: Q8041560
→ subclass of (P279)polymalformative genetic syndrome with increased risk of developing cancerObserved
Relationship details
Provider: Wikidata · Property: P279 · Direction: outgoing · Entity ID: Q55785832

Other connections (11)

→ Relationship name unavailable (P2888)http://www.orpha.net/ORDO/Orphanet_50Observed
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 (P689)Homo sapiensObserved
Relationship details
Provider: Wikidata · Property: P689 · Direction: outgoing · Entity ID: Q15978631
→ Relationship name unavailable (P1995)medical geneticsObserved
Relationship details
Provider: Wikidata · Property: P1995 · Direction: outgoing · Entity ID: Q1071953
→ Relationship name unavailable (P667)N85Observed
Relationship details
Provider: Wikidata · Property: P667 · Direction: outgoing
→ Relationship name unavailable (P1325)http://www.nanbyou.or.jp/entry/4393Observed
Relationship details
Provider: Wikidata · Property: P1325 · Direction: outgoing
→ Relationship name unavailable (P2888)http://identifiers.org/doid/DOID:8461Observed
Relationship details
Provider: Wikidata · Property: P2888 · Direction: outgoing
→ Relationship name unavailable (P2888)http://purl.obolibrary.org/obo/DOID_8461Observed
Relationship details
Provider: Wikidata · Property: P2888 · Direction: outgoing
→ Relationship name unavailable (P5008)WikiProject MedicineObserved
Relationship details
Provider: Wikidata · Property: P5008 · Direction: outgoing · Entity ID: Q4099686
→ different from (P1889)Aicardi-Goutieres syndromeObserved
Relationship details
Provider: Wikidata · Property: P1889 · Direction: outgoing · Entity ID: Q403453
← different from (P1889)Aicardi-Goutieres syndromeObserved
Relationship details
Provider: Wikidata · Property: P1889 · Direction: incoming · Entity ID: Q403453

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