Wikimedia neighborhood · Wikidata observation Observed Graph-projection

hypoparathyroidism-deafness-renal disease syndrome

characterized by autosomal dominant inheritance of hypoparathyroidism, sensorineural deafness and progressive renal failure that has material basis in chromosome deletion that results in haploinsufficiency of the GATA3 gene on chromosome 10p14

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

Data and provenance

Provider: Wikidata · Entity ID: Q2027515

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)

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 (9)

→ subclass of (P279)chromosomal deletion syndromeObserved
Relationship details
Provider: Wikidata · Property: P279 · Direction: outgoing · Entity ID: Q16918398
→ subclass of (P279)syndromic genetic deafnessObserved
Relationship details
Provider: Wikidata · Property: P279 · Direction: outgoing · Entity ID: Q55788734
→ subclass of (P279)syndromic renal or urinary tract malformationObserved
Relationship details
Provider: Wikidata · Property: P279 · Direction: outgoing · Entity ID: Q55788832
→ instance of (P31)type of diseaseObserved
Relationship details
Provider: Wikidata · Property: P31 · Direction: outgoing · Entity ID: Q112193867
→ subclass of (P279)syndrome with hypoparathyroidismObserved
Relationship details
Provider: Wikidata · Property: P279 · Direction: outgoing · Entity ID: Q55785800
→ instance of (P31)rare diseaseObserved
Relationship details
Provider: Wikidata · Property: P31 · Direction: outgoing · Entity ID: Q929833
→ subclass of (P279)head and neck diseaseObserved
Relationship details
Provider: Wikidata · Property: P279 · Direction: outgoing · Entity ID: Q55789477
→ subclass of (P279)developmental defect during embryogenesisObserved
Relationship details
Provider: Wikidata · Property: P279 · Direction: outgoing · Entity ID: Q55788864
→ subclass of (P279)partial deletion of the short arm of chromosome 10Observed
Relationship details
Provider: Wikidata · Property: P279 · Direction: outgoing · Entity ID: Q55786595

Other connections (8)

→ Relationship name unavailable (P1995)medical geneticsObserved
Relationship details
Provider: Wikidata · Property: P1995 · Direction: outgoing · Entity ID: Q1071953
→ Relationship name unavailable (P2888)http://www.orpha.net/ORDO/Orphanet_2237Observed
Relationship details
Provider: Wikidata · Property: P2888 · Direction: outgoing
→ Relationship name unavailable (P2293)GATA3Observed
Relationship details
Provider: Wikidata · Property: P2293 · Direction: outgoing · Entity ID: Q18025464
→ Relationship name unavailable (P2888)http://purl.obolibrary.org/obo/DOID_0060878Observed
Relationship details
Provider: Wikidata · Property: P2888 · Direction: outgoing
→ named after (P138)Amin J. BarakatObserved
Relationship details
Provider: Wikidata · Property: P138 · Direction: outgoing · Entity ID: Q4746312
→ Relationship name unavailable (P2888)http://identifiers.org/doid/DOID:0060878Observed
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
← Relationship name unavailable (P2293)GATA3Observed
Relationship details
Provider: Wikidata · Property: P2293 · Direction: incoming · Entity ID: Q18025464

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