(Q21505526)

English

myopathy, lactic acidosis, and sideroblastic anemia

Human disease

MLASA
mitochondrial myopathy and sideroblastic anemia

In more languages

Statements

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class of disease

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muscular disease

1 reference

Disease Ontology

15 May 2019

Disease Ontology ID

mitochondrial myopathy

1 reference

Disease Ontology

29 November 2020

Disease Ontology ID

symptoms and signs

sideroblastic anaemia P

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genetic association

1 reference

Missense mutation in pseudouridine synthase 1 (PUS1) causes mitochondrial myopathy and sideroblastic anemia (MLASA).

1 reference

Mutation of the mitochondrial tyrosyl-tRNA synthetase gene, YARS2, causes myopathy, lactic acidosis, and sideroblastic anemia--MLASA syndrome

on focus list of Wikimedia project

WikiProject Medicine

0 references

http://purl.obolibrary.org/obo/DOID_0080099

1 reference

Disease Ontology

29 November 2020

Disease Ontology ID

http://identifiers.org/doid/DOID:0080099

1 reference

Identifiers.org

https://registry.identifiers.org/registry/doid

Identifiers

MeSH descriptor ID

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Disease Ontology ID

1 reference

Disease Ontology

29 November 2020

Disease Ontology ID

GARD rare disease ID

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Google Knowledge Graph ID

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ICD-11 (foundation)

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1 reference

Disease Ontology

15 May 2019

Disease Ontology ID

1 reference

Disease Ontology

15 May 2019

Disease Ontology ID

1 reference

Disease Ontology

15 May 2019

Disease Ontology ID

0 references

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Sitelinks

Wikipedia(1 entry)

dewiki MLASA

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

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