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hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase

human disease
MedicalCondition rare_disease Q32146367
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hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase

Summary

hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase is a rare disease[1].

Key Facts

  • hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase's instance of is recorded as rare disease[2].
  • hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase's instance of is recorded as class of disease[3].
  • hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase's subclass of is recorded as hypermethioninemia[4].
  • hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase's subclass of is recorded as sulfuraminoacidemia[5].
  • hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase's subclass of is recorded as genetic syndromic intellectual disability[6].
  • hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase's OMIM ID is recorded as 613752[7].
  • hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase's Disease Ontology ID is recorded as DOID:0111039[8].
  • hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase's Orphanet ID is recorded as 88618[9].
  • hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase's genetic association is recorded as AHCY[10].
  • hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111039[11].
  • hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase's exact match is recorded as http://identifiers.org/doid/DOID:0111039[12].
  • hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_88618[13].
  • hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase's UMLS CUI is recorded as C3151058[14].
  • hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase's ICD-10-CM is recorded as E72.1[15].
  • hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase's GARD rare disease ID is recorded as 13177[16].
  • hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase's on focus list of Wikimedia project is recorded as WikiProject Medicine[17].
  • hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase's Mondo ID is recorded as MONDO_0013404[18].
  • hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase's UniProt disease ID is recorded as DI-01774[19].

References

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

Direct Wikidata claims

  1. [2] ↑ . wikidata.org.
  2. [3] ↑ . wikidata.org.
  3. [4] ↑ . Disease Ontology. Retrieved . wikidata.org.
  4. [5] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  5. [6] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  6. [7] ↑ . Disease Ontology. Retrieved . wikidata.org.
  7. [8] ↑ . Disease Ontology. Retrieved . wikidata.org.
  8. [9] ↑ . Disease Ontology. Retrieved . wikidata.org.
  9. [10] ↑ . Q905695. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  10. [11] ↑ . Disease Ontology. Retrieved . wikidata.org.
  11. [12] ↑ . Identifiers.org. ebi.ac.uk. Provenance: wikidata.org.
  12. [13] ↑ . wikidata.org.
  13. [14] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  14. [15] ↑ . Disease Ontology. Retrieved . wikidata.org.
  15. [16] ↑ . Disease Ontology. Retrieved . wikidata.org.
  16. [17] ↑ . wikidata.org.
  17. [18] ↑ . wikidata.org.
  18. [19] ↑ . 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). hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase. Retrieved May 3, 2026, from https://4ort.xyz/entity/hypermethioninemia-with-deficiency-of-s-adenosylhomocysteine-hydrolase
MLA “hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/hypermethioninemia-with-deficiency-of-s-adenosylhomocysteine-hydrolase.
BibTeX @misc{4ortxyz_hypermethioninemia-with-deficiency-of-s-adenosylhomocysteine-hydrolase_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase}}, year = {2026}, url = {https://4ort.xyz/entity/hypermethioninemia-with-deficiency-of-s-adenosylhomocysteine-hydrolase}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase — https://4ort.xyz/entity/hypermethioninemia-with-deficiency-of-s-adenosylhomocysteine-hydrolase (retrieved 2026-05-03)

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