hereditary spherocytosis type 3

hereditary spherocytosis that has material basis in an autosomal dominant mutation of SPTA1 on chromosome 1q23.1

Class type of: hereditary spherocytosis, genetic disease, autosomal recessive disease Q32144729

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Summary

hereditary spherocytosis type 3 is a class of disease^[1]. It is a type of hereditary spherocytosis^[2], genetic disease^[3], and autosomal recessive disease^[4].

Key Facts

Genetic association: SPTA1^[5]
On focus list of Wikimedia project: WikiProject Medicine^[6]

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Quick Facts

Instance of class of disease

Subclass of hereditary spherocytosis, genetic disease, autosomal recessive disease

Properties

Genetic association SPTA1

On focus list of wikimedia project WikiProject Medicine

Identifiers (7)

Disease ontology id DOID:0110918

Exact match purl.obolibrary.org, identifiers.org, www.orpha.net

Mesh descriptor id C567489

Mondo id MONDO_0010053

Omim id 270970

Umls cui C2678338

Uniprot disease id DI-02323

🏷️ Also known as

en hereditary spherocytosis 3 en hereditary spherocytosis type 3 en HS3 en SPH3 en Spherocytosis, Hereditary, 3 en SPHEROCYTOSIS, TYPE 3 en SPHEROCYTOSIS, TYPE 3; SPH3

References

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

Direct Wikidata claims

[2] ↑ hereditary spherocytosis type 3 — subclass of (P279): hereditary spherocytosis. Disease Ontology. Retrieved 2020-11-30. wikidata.org.
[3] ↑ hereditary spherocytosis type 3 — subclass of (P279): genetic disease. Disease Ontology. Retrieved 2019-05-15. wikidata.org.
[4] ↑ hereditary spherocytosis type 3 — subclass of (P279): autosomal recessive disease. Disease Ontology. Retrieved 2020-11-30. wikidata.org.
[5] ↑ hereditary spherocytosis type 3 — genetic association (P2293): SPTA1. UniProt. Retrieved 2019-08-13. wikidata.org.
[6] ↑ hereditary spherocytosis type 3 — on focus list of Wikimedia project (P5008): WikiProject Medicine. wikidata.org.

Class ancestry

[1] ↑ hereditary spherocytosis type 3 is an instance of class of disease (Q112193867) [P31, primary]. Wikidata. 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). hereditary spherocytosis type 3. Retrieved October 30, 2026, from https://4ort.xyz/entity/hereditary-spherocytosis-type-3

MLA

“hereditary spherocytosis type 3.” 4ort.xyz Knowledge Graph, 4ort.xyz, 30 Oct. 2026, https://4ort.xyz/entity/hereditary-spherocytosis-type-3.

BibTeX

@misc{4ortxyz_hereditary-spherocytosis-type-3_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{hereditary spherocytosis type 3}}, year = {2026}, url = {https://4ort.xyz/entity/hereditary-spherocytosis-type-3}, note = {Accessed: 2026-10-30}}

LLM prompt

According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): hereditary spherocytosis type 3 — https://4ort.xyz/entity/hereditary-spherocytosis-type-3 (retrieved 2026-10-30)

Canonical URL: https://4ort.xyz/entity/hereditary-spherocytosis-type-3 · Last refreshed: October 30, 2026

Edit History

Rolling log of changes to this entity's Wikidata record. Values shown reflect the current state of each edited property — follow the history link to see the precise diff for any edit.

17w ago · JhealdBatch bot · 2026-07-05 view diff on Wikidata ↗

Mondo id → MONDO_0010053

Imported from → —

Umls cui → C2678338

Disease ontology id → DOID:0110918

+ 9 other properties edited (see Wikidata diff for full list)

"/* wbeditentity-update:0| */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/39943|batch #39943]]: deprecate redundant disease superclasses"

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