succinic semialdehyde dehydrogenase deficiency

Rare disorder involving deficiency in GABA degradation
MedicalCondition rare_disease Q2823333
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succinic semialdehyde dehydrogenase deficiency

Summary

succinic semialdehyde dehydrogenase deficiency is a rare disease[1]. It draws 32 Wikipedia views per month (rare_disease category, ranking #206 of 627).[2]

Key Facts

  • succinic semialdehyde dehydrogenase deficiency's instance of is recorded as rare disease[3].
  • succinic semialdehyde dehydrogenase deficiency's instance of is recorded as class of disease[4].
  • succinic semialdehyde dehydrogenase deficiency's subclass of is recorded as gamma-amino butyric acid metabolism disorder[5].
  • succinic semialdehyde dehydrogenase deficiency's subclass of is recorded as metabolic neurotransmission anomaly with epilepsy[6].
  • succinic semialdehyde dehydrogenase deficiency's subclass of is recorded as rare genetic epilepsy[7].
  • succinic semialdehyde dehydrogenase deficiency's subclass of is recorded as neurometabolic disease[8].
  • succinic semialdehyde dehydrogenase deficiency's MeSH descriptor ID is recorded as C535803[9].
  • succinic semialdehyde dehydrogenase deficiency's OMIM ID is recorded as 271980[10].
  • succinic semialdehyde dehydrogenase deficiency's DiseasesDB is recorded as 29825[11].
  • succinic semialdehyde dehydrogenase deficiency's KEGG ID is recorded as H00835[12].
  • succinic semialdehyde dehydrogenase deficiency's Disease Ontology ID is recorded as DOID:0060175[13].
  • succinic semialdehyde dehydrogenase deficiency's Orphanet ID is recorded as 22[14].
  • succinic semialdehyde dehydrogenase deficiency's genetic association is recorded as ALDH5A1[15].
  • succinic semialdehyde dehydrogenase deficiency's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060175[16].
  • succinic semialdehyde dehydrogenase deficiency's exact match is recorded as http://identifiers.org/doid/DOID:0060175[17].
  • succinic semialdehyde dehydrogenase deficiency's UMLS CUI is recorded as C0268631[18].
  • succinic semialdehyde dehydrogenase deficiency's ICD-10-CM is recorded as E72.8[19].
  • succinic semialdehyde dehydrogenase deficiency's GARD rare disease ID is recorded as 7695[20].
  • succinic semialdehyde dehydrogenase deficiency's on focus list of Wikimedia project is recorded as WikiProject Medicine[21].
  • succinic semialdehyde dehydrogenase deficiency's Mondo ID is recorded as MONDO_0010083[22].
  • succinic semialdehyde dehydrogenase deficiency's Microsoft Academic ID is recorded as 2778085857[23].
  • succinic semialdehyde dehydrogenase deficiency's Genetics Home Reference Conditions ID is recorded as succinic-semialdehyde-dehydrogenase-deficiency[24].
  • succinic semialdehyde dehydrogenase deficiency's WikiProjectMed ID is recorded as Succinic semialdehyde dehydrogenase deficiency[25].
  • succinic semialdehyde dehydrogenase deficiency's UniProt disease ID is recorded as DI-02345[26].

Why It Matters

succinic semialdehyde dehydrogenase deficiency draws 32 Wikipedia views per month (rare_disease category, ranking #206 of 627).[2] It has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[27] It is known by 11 alternative names across languages and contexts.[28]

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

Class ancestry

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

Aggregate / graph-position facts

  1. [2] . Wikimedia Foundation. dumps.wikimedia.org.
  2. [27] . Wikidata sitelinks. wikidata.org.
  3. [28] . 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). succinic semialdehyde dehydrogenase deficiency. Retrieved May 3, 2026, from https://4ort.xyz/entity/succinic-semialdehyde-dehydrogenase-deficiency
MLA “succinic semialdehyde dehydrogenase deficiency.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/succinic-semialdehyde-dehydrogenase-deficiency.
BibTeX @misc{4ortxyz_succinic-semialdehyde-dehydrogenase-deficiency_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{succinic semialdehyde dehydrogenase deficiency}}, year = {2026}, url = {https://4ort.xyz/entity/succinic-semialdehyde-dehydrogenase-deficiency}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): succinic semialdehyde dehydrogenase deficiency — https://4ort.xyz/entity/succinic-semialdehyde-dehydrogenase-deficiency (retrieved 2026-05-03)

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