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syndactyly type 8

human disease
MedicalCondition developmental_defect_during_embryogenesis Q55782588
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syndactyly type 8

Summary

syndactyly type 8 is a developmental defect during embryogenesis[1]. It is known by 7 alternative names across languages and contexts.[2]

Key Facts

  • syndactyly type 8's instance of is recorded as developmental defect during embryogenesis[3].
  • syndactyly type 8's instance of is recorded as syndactyly[4].
  • syndactyly type 8's instance of is recorded as rare disease[5].
  • syndactyly type 8's instance of is recorded as class of disease[6].
  • syndactyly type 8 is a type of syndactyly[7].
  • syndactyly type 8 is a type of X-linked recessive disease[8].
  • syndactyly type 8's genetic association is recorded as FGF16[9].
  • syndactyly type 8's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2498[10].
  • syndactyly type 8's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111813[11].
  • syndactyly type 8's exact match is recorded as http://identifiers.org/doid/DOID:0111813[12].

Why It Matters

syndactyly type 8 is known by 7 alternative names across languages and contexts.[2]

References

Programmatic citations — every numbered marker resolves to a verifiable graph row below.

Direct Wikidata claims

  1. [3] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  2. [4] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  3. [5] ↑ . wikidata.org.
  4. [6] ↑ . wikidata.org.
  5. [7] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  6. [8] ↑ . Disease Ontology. Retrieved . wikidata.org.
  7. [9] ↑ . Q905695. Retrieved . wikidata.org.
  8. [10] ↑ . wikidata.org.
  9. [11] ↑ . Disease Ontology. Retrieved . wikidata.org.
  10. [12] ↑ . Identifiers.org. registry.identifiers.org. Provenance: wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] ↑ . Wikidata aliases. wikidata.org.

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APA 4ort.xyz Knowledge Graph. (2026). syndactyly type 8. Retrieved May 3, 2026, from https://4ort.xyz/entity/syndactyly-type-8
MLA “syndactyly type 8.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/syndactyly-type-8.
BibTeX @misc{4ortxyz_syndactyly-type-8_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{syndactyly type 8}}, year = {2026}, url = {https://4ort.xyz/entity/syndactyly-type-8}, note = {Accessed: 2026-05-03}}
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Edit History

Rolling log of changes to this entity's Wikidata record. Values shown reflect the current state of each edited property — follow the history link to see the precise diff for any edit.

  1. 8w ago · KrBot bot · 2026-07-23 view diff on Wikidata ↗
    Subclass of → syndactyly, X-linked recessive disease
    "/* wbremoveclaims-remove:1| */ [[Property:P279]]: [[Q1360044]], дублирующееся значение / duplicate value"
  2. 11w ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Mondo id → MONDO_0010669
    Genetic association → FGF16
    Gard rare disease id → 3559
    Orphanet id → 2498
    + 11 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/39742|batch #39742]]: subclass of disease, not instance"
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