biotinidase deficiency

multiple carboxylase deficiency that involves a deficiency in biotinidase
MedicalCondition class_of_disease Q776026
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biotinidase deficiency

Summary

biotinidase deficiency is a class of disease[1]. It draws 20 Wikipedia views per month (class_of_disease category, ranking #612 of 1,968).[2]

Key Facts

  • biotinidase deficiency's image is recorded as Biotin structure.svg[3].
  • biotinidase deficiency's instance of is recorded as class of disease[4].
  • biotinidase deficiency's subclass of is recorded as multiple carboxylase deficiency[5].
  • biotinidase deficiency's subclass of is recorded as disorder of other vitamins and cofactors metabolism and transport[6].
  • biotinidase deficiency's subclass of is recorded as rare genetic epilepsy[7].
  • biotinidase deficiency's subclass of is recorded as rare hereditary metabolic disease with peripheral neuropathy[8].
  • biotinidase deficiency's MeSH descriptor ID is recorded as D028921[9].
  • biotinidase deficiency's OMIM ID is recorded as 253260[10].
  • biotinidase deficiency's ICD-9 ID is recorded as 277.6[11].
  • biotinidase deficiency's DiseasesDB is recorded as 29822[12].
  • biotinidase deficiency's Freebase ID is recorded as /m/08wflp[13].
  • biotinidase deficiency's KEGG ID is recorded as H01182[14].
  • biotinidase deficiency's MeSH tree code is recorded as C16.320.565.100.620.100[15].
  • biotinidase deficiency's MeSH tree code is recorded as C16.320.565.202.720.100[16].
  • biotinidase deficiency's MeSH tree code is recorded as C18.452.648.100.620.100[17].
  • biotinidase deficiency's MeSH tree code is recorded as C18.452.648.202.720.100[18].
  • biotinidase deficiency's eMedicine ID is recorded as 942055[19].
  • biotinidase deficiency's Disease Ontology ID is recorded as DOID:856[20].
  • biotinidase deficiency's Orphanet ID is recorded as 79241[21].
  • biotinidase deficiency's ICD-9-CM is recorded as 277.6[22].
  • biotinidase deficiency's NCI Thesaurus ID is recorded as C84598[23].
  • biotinidase deficiency's health specialty is recorded as endocrinology[24].
  • biotinidase deficiency's genetic association is recorded as BTD[25].
  • biotinidase deficiency's exact match is recorded as http://purl.obolibrary.org/obo/DOID_856[26].
  • biotinidase deficiency's exact match is recorded as http://identifiers.org/doid/DOID:856[27].

Why It Matters

biotinidase deficiency draws 20 Wikipedia views per month (class_of_disease category, ranking #612 of 1,968).[2] It has Wikipedia articles in 8 language editions, a strong signal of global cultural recognition.[28] It is known by 7 alternative names across languages and contexts.[29]

References

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

Direct Wikidata claims

  1. [3] . wikidata.org.
  2. [4] . wikidata.org.
  3. [5] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  4. [6] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  5. [7] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  6. [8] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  7. [9] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  8. [10] . Disease Ontology. Retrieved . wikidata.org.
  9. [11] . wikidata.org.
  10. [12] . wikidata.org.
  11. [13] . Freebase Data Dumps. wikidata.org.
  12. [14] . wikidata.org.
  13. [15] . wikidata.org.
  14. [16] . wikidata.org.
  15. [17] . wikidata.org.
  16. [18] . wikidata.org.
  17. [19] . wikidata.org.
  18. [20] . Disease Ontology. Retrieved . wikidata.org.
  19. [21] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  20. [22] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  21. [23] . Disease Ontology. Retrieved . wikidata.org.
  22. [24] . wikidata.org.
  23. [25] . Q905695. Retrieved . search.clinicalgenome.org. Provenance: wikidata.org.
  24. [26] . Disease Ontology. Retrieved . wikidata.org.
  25. [27] . Identifiers.org. registry.identifiers.org. Provenance: wikidata.org.

Class ancestry

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

Aggregate / graph-position facts

  1. [2] . Wikimedia Foundation. dumps.wikimedia.org.
  2. [28] . Wikidata sitelinks. wikidata.org.
  3. [29] . Wikidata aliases. 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). biotinidase deficiency. Retrieved May 3, 2026, from https://4ort.xyz/entity/biotinidase-deficiency
MLA “biotinidase deficiency.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/biotinidase-deficiency.
BibTeX @misc{4ortxyz_biotinidase-deficiency_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{biotinidase deficiency}}, year = {2026}, url = {https://4ort.xyz/entity/biotinidase-deficiency}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): biotinidase deficiency — https://4ort.xyz/entity/biotinidase-deficiency (retrieved 2026-05-03)

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