multiple carboxylase deficiency

human disease
MedicalCondition designated_intractable_rare_disease Q6934914
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multiple carboxylase deficiency

Summary

multiple carboxylase deficiency is a designated intractable/rare disease[1].

Key Facts

  • multiple carboxylase deficiency's instance of is recorded as designated intractable/rare disease[2].
  • multiple carboxylase deficiency's instance of is recorded as class of disease[3].
  • multiple carboxylase deficiency's subclass of is recorded as carbohydrate metabolic disorder[4].
  • multiple carboxylase deficiency's subclass of is recorded as amino acid metabolic disorder[5].
  • multiple carboxylase deficiency's subclass of is recorded as classic organic aciduria[6].
  • multiple carboxylase deficiency's subclass of is recorded as other metabolic disease with skin involvement[7].
  • multiple carboxylase deficiency's subclass of is recorded as vitamin metabolic disorder[8].
  • multiple carboxylase deficiency's MeSH descriptor ID is recorded as D009100[9].
  • multiple carboxylase deficiency's MeSH tree code is recorded as C16.320.565.100.620[10].
  • multiple carboxylase deficiency's MeSH tree code is recorded as C16.320.565.202.720[11].
  • multiple carboxylase deficiency's MeSH tree code is recorded as C18.452.648.100.620[12].
  • multiple carboxylase deficiency's MeSH tree code is recorded as C18.452.648.202.720[13].
  • multiple carboxylase deficiency's Disease Ontology ID is recorded as DOID:857[14].
  • multiple carboxylase deficiency's external data available at URL is recorded as http://www.nanbyou.or.jp/entry/4825[15].
  • multiple carboxylase deficiency's Orphanet ID is recorded as 148[16].
  • multiple carboxylase deficiency's health specialty is recorded as medical genetics[17].
  • multiple carboxylase deficiency's health specialty is recorded as endocrinology[18].
  • multiple carboxylase deficiency's exact match is recorded as http://purl.obolibrary.org/obo/DOID_857[19].
  • multiple carboxylase deficiency's exact match is recorded as http://identifiers.org/doid/DOID:857[20].
  • multiple carboxylase deficiency's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_148[21].
  • multiple carboxylase deficiency's UMLS CUI is recorded as C0026755[22].
  • multiple carboxylase deficiency's ICD-10-CM is recorded as D81.819[23].
  • multiple carboxylase deficiency's ICD-10-CM is recorded as D81.81[24].
  • multiple carboxylase deficiency's ICD-10-CM is recorded as E53.8[25].
  • multiple carboxylase deficiency's GARD rare disease ID is recorded as 3824[26].

References

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

Direct Wikidata claims

  1. [2] . ddrare.nibiohn.go.jp. Retrieved . ddrare.nibiohn.go.jp. Provenance: wikidata.org.
  2. [3] . wikidata.org.
  3. [4] . Disease Ontology. Retrieved . wikidata.org.
  4. [5] . Disease Ontology. Retrieved . wikidata.org.
  5. [6] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  6. [7] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  7. [8] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  8. [9] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  9. [10] . wikidata.org.
  10. [11] . wikidata.org.
  11. [12] . wikidata.org.
  12. [13] . wikidata.org.
  13. [14] . Disease Ontology. Retrieved . wikidata.org.
  14. [15] . ddrare.nibiohn.go.jp. Retrieved . ddrare.nibiohn.go.jp. Provenance: wikidata.org.
  15. [16] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  16. [17] . wikidata.org.
  17. [18] . wikidata.org.
  18. [19] . Disease Ontology. Retrieved . wikidata.org.
  19. [20] . Disease Ontology. Retrieved . registry.identifiers.org. Provenance: wikidata.org.
  20. [21] . wikidata.org.
  21. [22] . Disease Ontology. Retrieved . wikidata.org.
  22. [23] . Disease Ontology. Retrieved . wikidata.org.
  23. [24] . Disease Ontology. Retrieved . wikidata.org.
  24. [25] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  25. [26] . Disease Ontology. Retrieved . wikidata.org.

Class ancestry

  1. [1] . Wikidata. wikidata.org.

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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). multiple carboxylase deficiency. Retrieved May 3, 2026, from https://4ort.xyz/entity/multiple-carboxylase-deficiency
MLA “multiple carboxylase deficiency.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/multiple-carboxylase-deficiency.
BibTeX @misc{4ortxyz_multiple-carboxylase-deficiency_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{multiple carboxylase deficiency}}, year = {2026}, url = {https://4ort.xyz/entity/multiple-carboxylase-deficiency}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): multiple carboxylase deficiency — https://4ort.xyz/entity/multiple-carboxylase-deficiency (retrieved 2026-05-03)

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