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amelogenesis imperfecta, type IJ; AI1J

human disease
MedicalCondition rare_disease Q55785177
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amelogenesis imperfecta, type IJ; AI1J

Summary

amelogenesis imperfecta, type IJ; AI1J is a rare disease[1].

Key Facts

  • amelogenesis imperfecta, type IJ; AI1J's instance of is recorded as rare disease[2].
  • amelogenesis imperfecta, type IJ; AI1J's instance of is recorded as disease[3].
  • amelogenesis imperfecta, type IJ; AI1J's instance of is recorded as class of disease[4].
  • amelogenesis imperfecta, type IJ; AI1J is a type of genetic disease[5].
  • amelogenesis imperfecta, type IJ; AI1J is a type of amelogenesis imperfecta[6].
  • amelogenesis imperfecta, type IJ; AI1J is a type of autosomal recessive disease[7].
  • amelogenesis imperfecta, type IJ; AI1J's genetic association is recorded as ACP4[8].
  • amelogenesis imperfecta, type IJ; AI1J's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0080953[9].
  • amelogenesis imperfecta, type IJ; AI1J's exact match is recorded as http://identifiers.org/doid/DOID:0080953[10].

References

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

Direct Wikidata claims

  1. [2] ↑ . wikidata.org.
  2. [3] ↑ . Amelogenesis imperfecta, dentinogenesis imperfecta and dentin dysplasia revisited: problems in classification. wikidata.org.
  3. [4] ↑ . wikidata.org.
  4. [5] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  5. [6] ↑ . Disease Ontology. Retrieved . wikidata.org.
  6. [7] ↑ . Disease Ontology. Retrieved . wikidata.org.
  7. [8] ↑ . Recessive Mutations in ACPT, Encoding Testicular Acid Phosphatase, Cause Hypoplastic Amelogenesis Imperfecta. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  8. [9] ↑ . Disease Ontology. Retrieved . wikidata.org.
  9. [10] ↑ . Identifiers.org. registry.identifiers.org. Provenance: wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

📑 Cite this page

Use these citations when quoting this entity in research, articles, AI prompts, or wherever provenance matters. We aggregate Wikidata + Wikipedia + authoritative open-data sources; the stitched, scored, cross-referenced view is what 4ort.xyz contributes.

APA 4ort.xyz Knowledge Graph. (2026). amelogenesis imperfecta, type IJ; AI1J. Retrieved May 3, 2026, from https://4ort.xyz/entity/amelogenesis-imperfecta-type-ij-ai1j
MLA “amelogenesis imperfecta, type IJ; AI1J.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/amelogenesis-imperfecta-type-ij-ai1j.
BibTeX @misc{4ortxyz_amelogenesis-imperfecta-type-ij-ai1j_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{amelogenesis imperfecta, type IJ; AI1J}}, year = {2026}, url = {https://4ort.xyz/entity/amelogenesis-imperfecta-type-ij-ai1j}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): amelogenesis imperfecta, type IJ; AI1J — https://4ort.xyz/entity/amelogenesis-imperfecta-type-ij-ai1j (retrieved 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. 14w ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Mondo id → MONDO_0015008
    Genetic association → ACP4
    Instance of → rare disease, disease, class of disease
    Experimental factor ontology id → 0009302
    + 8 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/39731|batch #39731]]: rm redundant P31"
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