hemochromatosis type 2

hemochromatosis characterized by autosomal recessive inheritance of early onset of severe iron loading with symptoms including; hypogonadotropic hypogonadism, cardiomyopathy, arthropathy, and liver fibrosis or cirrhosis
MedicalCondition class_of_disease Q6318953
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hemochromatosis type 2

Summary

hemochromatosis type 2 is a class of disease[1]. It draws 9 Wikipedia views per month (class_of_disease category, ranking #624 of 1,968).[2]

Key Facts

  • hemochromatosis type 2's instance of is recorded as class of disease[3].
  • hemochromatosis type 2's subclass of is recorded as iron overload[4].
  • hemochromatosis type 2's subclass of is recorded as hereditary haemochromatosis[5].
  • hemochromatosis type 2's MeSH descriptor ID is recorded as C537247[6].
  • hemochromatosis type 2's OMIM ID is recorded as 602390[7].
  • hemochromatosis type 2's ICD-9 ID is recorded as 275.0[8].
  • hemochromatosis type 2's Disease Ontology ID is recorded as DOID:0111034[9].
  • hemochromatosis type 2's Encyclopædia Britannica Online ID is recorded as topic/type-2-hemochromatosis[10].
  • hemochromatosis type 2's Orphanet ID is recorded as 79230[11].
  • hemochromatosis type 2's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111034[12].
  • hemochromatosis type 2's exact match is recorded as http://identifiers.org/doid/DOID:0111034[13].
  • hemochromatosis type 2's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_79230[14].
  • hemochromatosis type 2's UMLS CUI is recorded as C0268060[15].
  • hemochromatosis type 2's ICD-10-CM is recorded as E83.1[16].
  • hemochromatosis type 2's GARD rare disease ID is recorded as 10092[17].
  • hemochromatosis type 2's on focus list of Wikimedia project is recorded as WikiProject Medicine[18].
  • hemochromatosis type 2's Microsoft Academic ID is recorded as 2780426346[19].
  • hemochromatosis type 2's WikiProjectMed ID is recorded as Juvenile hemochromatosis[20].

Why It Matters

hemochromatosis type 2 draws 9 Wikipedia views per month (class_of_disease category, ranking #624 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] . Disease Ontology. Retrieved . wikidata.org.
  4. [6] . Disease Ontology. Retrieved . wikidata.org.
  5. [7] . wikidata.org.
  6. [8] . wikidata.org.
  7. [9] . Disease Ontology. Retrieved . wikidata.org.
  8. [10] . wikidata.org.
  9. [11] . Disease Ontology. Retrieved . wikidata.org.
  10. [12] . Disease Ontology. Retrieved . wikidata.org.
  11. [13] . Identifiers.org. registry.identifiers.org. Provenance: wikidata.org.
  12. [14] . wikidata.org.
  13. [15] . UMLS 2023. Retrieved . wikidata.org.
  14. [16] . Disease Ontology. Retrieved . wikidata.org.
  15. [17] . Disease Ontology. Retrieved . wikidata.org.
  16. [18] . wikidata.org.
  17. [19] . wikidata.org.
  18. [20] . 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). hemochromatosis type 2. Retrieved May 3, 2026, from https://4ort.xyz/entity/hemochromatosis-type-2
MLA “hemochromatosis type 2.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/hemochromatosis-type-2.
BibTeX @misc{4ortxyz_hemochromatosis-type-2_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{hemochromatosis type 2}}, year = {2026}, url = {https://4ort.xyz/entity/hemochromatosis-type-2}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): hemochromatosis type 2 — https://4ort.xyz/entity/hemochromatosis-type-2 (retrieved 2026-05-03)

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