autosomal recessive limb-girdle muscular dystrophy type 2F

autosomal recessive limb-girdle muscular dystrophy that has material basis in mutation in the sarcoglycan-delta gene (SGCD)

MedicalCondition rare_disease Q27677701

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autosomal recessive limb-girdle muscular dystrophy type 2F

Summary

autosomal recessive limb-girdle muscular dystrophy type 2F is a rare disease^[1].

Key Facts

autosomal recessive limb-girdle muscular dystrophy type 2F's instance of is recorded as rare disease^[2].
autosomal recessive limb-girdle muscular dystrophy type 2F's instance of is recorded as class of disease^[3].
autosomal recessive limb-girdle muscular dystrophy type 2F's subclass of is recorded as autosomal recessive limb-girdle muscular dystrophy^[4].
autosomal recessive limb-girdle muscular dystrophy type 2F's subclass of is recorded as sarcoglycanopathy^[5].
autosomal recessive limb-girdle muscular dystrophy type 2F's subclass of is recorded as qualitative or quantitative defects of delta-sarcoglycan^[6].
autosomal recessive limb-girdle muscular dystrophy type 2F's subclass of is recorded as neuromuscular disease with dilated cardiomyopathy^[7].
autosomal recessive limb-girdle muscular dystrophy type 2F's MeSH descriptor ID is recorded as C535896^[8].
autosomal recessive limb-girdle muscular dystrophy type 2F's OMIM ID is recorded as 601287^[9].
autosomal recessive limb-girdle muscular dystrophy type 2F's Disease Ontology ID is recorded as DOID:0110280^[10].
autosomal recessive limb-girdle muscular dystrophy type 2F's Orphanet ID is recorded as 219^[11].
autosomal recessive limb-girdle muscular dystrophy type 2F's health specialty is recorded as neurology^[12].
autosomal recessive limb-girdle muscular dystrophy type 2F's health specialty is recorded as myology^[13].
autosomal recessive limb-girdle muscular dystrophy type 2F's genetic association is recorded as SGCD^[14].
autosomal recessive limb-girdle muscular dystrophy type 2F's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110280^[15].
autosomal recessive limb-girdle muscular dystrophy type 2F's exact match is recorded as http://identifiers.org/doid/DOID:0110280^[16].
autosomal recessive limb-girdle muscular dystrophy type 2F's UMLS CUI is recorded as C1832525^[17].
autosomal recessive limb-girdle muscular dystrophy type 2F's ICD-10-CM is recorded as G71.0^[18].
autosomal recessive limb-girdle muscular dystrophy type 2F's GARD rare disease ID is recorded as 8573^[19].
autosomal recessive limb-girdle muscular dystrophy type 2F's on focus list of Wikimedia project is recorded as WikiProject Medicine^[20].
autosomal recessive limb-girdle muscular dystrophy type 2F's Mondo ID is recorded as MONDO_0011028^[21].

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Quick Facts

Instance of rare disease, class of disease

Subclass of autosomal recessive limb-girdle muscular dystrophy, sarcoglycanopathy, qualitative or quantitative defects of delta-sarcoglycan, neuromuscular disease with dilated cardiomyopathy

Properties

Exact match purl.obolibrary.org, identifiers.org

Genetic association SGCD

Health specialty neurology, myology

Imported from wholeness_audit_2026-05-02

On focus list of wikimedia project WikiProject Medicine

External References (8)

Disease ontology id DOID:0110280

Gard rare disease id 8573

Icd-10-cm G71.0

Mesh descriptor id C535896

Mondo id MONDO_0011028

Omim id 601287

Orphanet id 219

Umls cui C1832525

References

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

Direct Wikidata claims

[2] ↑ autosomal recessive limb-girdle muscular dystrophy type 2F — instance of (P31): rare disease. wikidata.org.
[3] ↑ autosomal recessive limb-girdle muscular dystrophy type 2F — instance of (P31): class of disease. wikidata.org.
[4] ↑ autosomal recessive limb-girdle muscular dystrophy type 2F — subclass of (P279): autosomal recessive limb-girdle muscular dystrophy. Monarch Disease Ontology release 2018-06-29. Retrieved 2018-07-28. wikidata.org.
[5] ↑ autosomal recessive limb-girdle muscular dystrophy type 2F — subclass of (P279): sarcoglycanopathy. wikidata.org.
[6] ↑ autosomal recessive limb-girdle muscular dystrophy type 2F — subclass of (P279): qualitative or quantitative defects of delta-sarcoglycan. Monarch Disease Ontology release 2018-06-29. Retrieved 2018-07-28. wikidata.org.
[7] ↑ autosomal recessive limb-girdle muscular dystrophy type 2F — subclass of (P279): neuromuscular disease with dilated cardiomyopathy. Monarch Disease Ontology release 2018-06-29. Retrieved 2018-07-28. wikidata.org.
[8] ↑ autosomal recessive limb-girdle muscular dystrophy type 2F — MeSH descriptor ID (P486): C535896. Monarch Disease Ontology release 2018-06-29. Retrieved 2018-07-28. wikidata.org.
[9] ↑ autosomal recessive limb-girdle muscular dystrophy type 2F — OMIM ID (P492): 601287. Disease Ontology. Retrieved 2019-08-28. wikidata.org.
[10] ↑ autosomal recessive limb-girdle muscular dystrophy type 2F — Disease Ontology ID (P699): DOID:0110280. Disease Ontology. Retrieved 2022-01-18. wikidata.org.
[11] ↑ autosomal recessive limb-girdle muscular dystrophy type 2F — Orphanet ID (P1550): 219. Disease Ontology. Retrieved 2019-08-28. wikidata.org.
[12] ↑ autosomal recessive limb-girdle muscular dystrophy type 2F — health specialty (P1995): neurology. wikidata.org.
[13] ↑ autosomal recessive limb-girdle muscular dystrophy type 2F — health specialty (P1995): myology. wikidata.org.
[14] ↑ autosomal recessive limb-girdle muscular dystrophy type 2F — genetic association (P2293): SGCD. Q905695. Retrieved 2019-08-13. platform.opentargets.org. Provenance: wikidata.org.
[15] ↑ autosomal recessive limb-girdle muscular dystrophy type 2F — exact match (P2888): http://purl.obolibrary.org/obo/DOID_0110280. Disease Ontology. Retrieved 2022-01-18. wikidata.org.
[16] ↑ autosomal recessive limb-girdle muscular dystrophy type 2F — exact match (P2888): http://identifiers.org/doid/DOID:0110280. Identifiers.org. registry.identifiers.org. Provenance: wikidata.org.
[17] ↑ autosomal recessive limb-girdle muscular dystrophy type 2F — UMLS CUI (P2892): C1832525. Monarch Disease Ontology release 2018-06-29. Retrieved 2018-07-28. wikidata.org.
[18] ↑ autosomal recessive limb-girdle muscular dystrophy type 2F — ICD-10-CM (P4229): G71.0. Disease Ontology. Retrieved 2019-08-28. wikidata.org.
[19] ↑ autosomal recessive limb-girdle muscular dystrophy type 2F — GARD rare disease ID (P4317): 8573. Monarch Disease Ontology release 2018-06-29. Retrieved 2018-07-28. wikidata.org.
[20] ↑ autosomal recessive limb-girdle muscular dystrophy type 2F — on focus list of Wikimedia project (P5008): WikiProject Medicine. wikidata.org.
[21] ↑ autosomal recessive limb-girdle muscular dystrophy type 2F — Mondo ID (P5270): MONDO_0011028. wikidata.org.

Class ancestry

[1] ↑ autosomal recessive limb-girdle muscular dystrophy type 2F is an instance of rare disease (Q929833) [P31, primary]. Wikidata. wikidata.org.

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APA

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MLA

“autosomal recessive limb-girdle muscular dystrophy type 2F.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/autosomal-recessive-limb-girdle-muscular-dystrophy-type-2f.

BibTeX

@misc{4ortxyz_autosomal-recessive-limb-girdle-muscular-dystrophy-type-2f_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{autosomal recessive limb-girdle muscular dystrophy type 2F}}, year = {2026}, url = {https://4ort.xyz/entity/autosomal-recessive-limb-girdle-muscular-dystrophy-type-2f}, note = {Accessed: 2026-05-03}}

LLM prompt

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