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3-hydroxy-3-methylglutaryl-CoA lyase deficiency

medical condition
MedicalCondition class_of_disease Q4634217
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Summary

3-hydroxy-3-methylglutaryl-CoA lyase deficiency is a class of disease[1]. It draws 1 Wikipedia views per month (class_of_disease category, ranking #631 of 1,968).[2]

Key Facts

  • 3-hydroxy-3-methylglutaryl-CoA lyase deficiency's instance of is recorded as class of disease[3].
  • 3-hydroxy-3-methylglutaryl-CoA lyase deficiency's subclass of is recorded as congenital disorder of amino acid metabolism[4].
  • 3-hydroxy-3-methylglutaryl-CoA lyase deficiency's subclass of is recorded as classic organic aciduria[5].
  • 3-hydroxy-3-methylglutaryl-CoA lyase deficiency's subclass of is recorded as disorder of fatty acid oxidation and ketogenesis[6].
  • 3-hydroxy-3-methylglutaryl-CoA lyase deficiency's MeSH descriptor ID is recorded as C538324[7].
  • 3-hydroxy-3-methylglutaryl-CoA lyase deficiency's OMIM ID is recorded as 246450[8].
  • 3-hydroxy-3-methylglutaryl-CoA lyase deficiency's DiseasesDB is recorded as 29826[9].
  • 3-hydroxy-3-methylglutaryl-CoA lyase deficiency's KEGG ID is recorded as H00179[10].
  • 3-hydroxy-3-methylglutaryl-CoA lyase deficiency's symptoms and signs is recorded as vomiting[11].
  • 3-hydroxy-3-methylglutaryl-CoA lyase deficiency's symptoms and signs is recorded as fatigue[12].
  • 3-hydroxy-3-methylglutaryl-CoA lyase deficiency's has cause is recorded as genetic disease[13].
  • 3-hydroxy-3-methylglutaryl-CoA lyase deficiency's possible treatment is recorded as diet[14].
  • 3-hydroxy-3-methylglutaryl-CoA lyase deficiency's Orphanet ID is recorded as 20[15].
  • 3-hydroxy-3-methylglutaryl-CoA lyase deficiency's NCI Thesaurus ID is recorded as C84523[16].
  • 3-hydroxy-3-methylglutaryl-CoA lyase deficiency's health specialty is recorded as pediatrics[17].
  • 3-hydroxy-3-methylglutaryl-CoA lyase deficiency's genetic association is recorded as HMGCL[18].
  • 3-hydroxy-3-methylglutaryl-CoA lyase deficiency's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_20[19].
  • 3-hydroxy-3-methylglutaryl-CoA lyase deficiency's UMLS CUI is recorded as C0268601[20].
  • 3-hydroxy-3-methylglutaryl-CoA lyase deficiency's UMLS CUI is recorded as C1415614[21].
  • 3-hydroxy-3-methylglutaryl-CoA lyase deficiency's UMLS CUI is recorded as C1533587[22].
  • 3-hydroxy-3-methylglutaryl-CoA lyase deficiency's ICD-10-CM is recorded as E71.1[23].
  • 3-hydroxy-3-methylglutaryl-CoA lyase deficiency's GARD rare disease ID is recorded as 8387[24].
  • 3-hydroxy-3-methylglutaryl-CoA lyase deficiency's Mondo ID is recorded as MONDO_0009520[25].
  • 3-hydroxy-3-methylglutaryl-CoA lyase deficiency's WikiProjectMed ID is recorded as 3-Hydroxy-3-methylglutaryl-CoA lyase deficiency[26].
  • 3-hydroxy-3-methylglutaryl-CoA lyase deficiency's UniProt disease ID is recorded as DI-00003[27].

Why It Matters

3-hydroxy-3-methylglutaryl-CoA lyase deficiency draws 1 Wikipedia views per month (class_of_disease category, ranking #631 of 1,968).[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] ↑ . 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] ↑ . wikidata.org.
  8. [10] ↑ . wikidata.org.
  9. [11] ↑ . wikidata.org.
  10. [12] ↑ . wikidata.org.
  11. [13] ↑ . wikidata.org.
  12. [14] ↑ . redalyc.org. redalyc.org. Provenance: wikidata.org.
  13. [15] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  14. [16] ↑ . wikidata.org.
  15. [17] ↑ . wikidata.org.
  16. [18] ↑ . UniProt. Retrieved . search.clinicalgenome.org. Provenance: wikidata.org.
  17. [19] ↑ . wikidata.org.
  18. [20] ↑ . Monarch Disease Ontology release 2018-06-29. 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] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  22. [24] ↑ . wikidata.org.
  23. [25] ↑ . 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.

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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). 3-hydroxy-3-methylglutaryl-CoA lyase deficiency. Retrieved October 18, 2026, from https://4ort.xyz/entity/3-hydroxy-3-methylglutaryl-coa-lyase-deficiency
MLA “3-hydroxy-3-methylglutaryl-CoA lyase deficiency.” 4ort.xyz Knowledge Graph, 4ort.xyz, 18 Oct. 2026, https://4ort.xyz/entity/3-hydroxy-3-methylglutaryl-coa-lyase-deficiency.
BibTeX @misc{4ortxyz_3-hydroxy-3-methylglutaryl-coa-lyase-deficiency_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{3-hydroxy-3-methylglutaryl-CoA lyase deficiency}}, year = {2026}, url = {https://4ort.xyz/entity/3-hydroxy-3-methylglutaryl-coa-lyase-deficiency}, note = {Accessed: 2026-10-18}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): 3-hydroxy-3-methylglutaryl-CoA lyase deficiency — https://4ort.xyz/entity/3-hydroxy-3-methylglutaryl-coa-lyase-deficiency (retrieved 2026-10-18)

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