carnitine palmitoyltransferase I deficiency

human disease
MedicalCondition rare_disease Q3043143
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carnitine palmitoyltransferase I deficiency

Summary

carnitine palmitoyltransferase I deficiency is a rare disease[1]. It draws 9 Wikipedia views per month (rare_disease category, ranking #233 of 627).[2]

Key Facts

  • carnitine palmitoyltransferase I deficiency's instance of is recorded as rare disease[3].
  • carnitine palmitoyltransferase I deficiency's instance of is recorded as class of disease[4].
  • carnitine palmitoyltransferase I deficiency's subclass of is recorded as lipid metabolism disorder[5].
  • carnitine palmitoyltransferase I deficiency's subclass of is recorded as disorder of carnitine cycle and carnitine transport[6].
  • carnitine palmitoyltransferase I deficiency's subclass of is recorded as genetic disease[7].
  • carnitine palmitoyltransferase I deficiency's MeSH descriptor ID is recorded as C535588[8].
  • carnitine palmitoyltransferase I deficiency's OMIM ID is recorded as 600528[9].
  • carnitine palmitoyltransferase I deficiency's OMIM ID is recorded as 255120[10].
  • carnitine palmitoyltransferase I deficiency's ICD-9 ID is recorded as 277.85[11].
  • carnitine palmitoyltransferase I deficiency's DiseasesDB is recorded as 32535[12].
  • carnitine palmitoyltransferase I deficiency's KEGG ID is recorded as H01981[13].
  • carnitine palmitoyltransferase I deficiency's eMedicine ID is recorded as 942233[14].
  • carnitine palmitoyltransferase I deficiency's Disease Ontology ID is recorded as DOID:0090129[15].
  • carnitine palmitoyltransferase I deficiency's Orphanet ID is recorded as 156[16].
  • carnitine palmitoyltransferase I deficiency's ICD-9-CM is recorded as 277.85[17].
  • carnitine palmitoyltransferase I deficiency's NCI Thesaurus ID is recorded as C98871[18].
  • carnitine palmitoyltransferase I deficiency's genetic association is recorded as CPT1A[19].
  • carnitine palmitoyltransferase I deficiency's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0090129[20].
  • carnitine palmitoyltransferase I deficiency's exact match is recorded as http://identifiers.org/doid/DOID:0090129[21].
  • carnitine palmitoyltransferase I deficiency's UMLS CUI is recorded as C0342789[22].
  • carnitine palmitoyltransferase I deficiency's UMLS CUI is recorded as C1829703[23].
  • carnitine palmitoyltransferase I deficiency's ICD-10-CM is recorded as E71.3[24].
  • carnitine palmitoyltransferase I deficiency's GARD rare disease ID is recorded as 1120[25].
  • carnitine palmitoyltransferase I deficiency's on focus list of Wikimedia project is recorded as WikiProject Medicine[26].
  • carnitine palmitoyltransferase I deficiency's Mondo ID is recorded as MONDO_0009705[27].

Why It Matters

carnitine palmitoyltransferase I deficiency draws 9 Wikipedia views per month (rare_disease category, ranking #233 of 627).[2]

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] . Disease Ontology. Retrieved . wikidata.org.
  4. [6] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  5. [7] . Disease Ontology. 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] . wikidata.org.
  12. [14] . wikidata.org.
  13. [15] . Disease Ontology. Retrieved . wikidata.org.
  14. [16] . Disease Ontology. Retrieved . wikidata.org.
  15. [17] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  16. [18] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  17. [19] . Q905695. Retrieved . search.clinicalgenome.org. Provenance: wikidata.org.
  18. [20] . Disease Ontology. Retrieved . wikidata.org.
  19. [21] . Identifiers.org. ebi.ac.uk. Provenance: wikidata.org.
  20. [22] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  21. [23] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  22. [24] . Disease Ontology. Retrieved . wikidata.org.
  23. [25] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  24. [26] . wikidata.org.
  25. [27] . wikidata.org.

Class ancestry

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

Aggregate / graph-position facts

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

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