(Q55786434)

English

maternally-inherited mitochondrial myopathy

human disease

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Statements

instance of

developmental defect during embryogenesis

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

28 July 2018

0 references

mitochondrial oxidative phosphorylation disorder due to a point mutation of mitochondrial DNA

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

retrieved

28 July 2018

Mondo ID

MONDO_0016794

mitochondrial myopathy

0 references

exact match

http://www.orpha.net/ORDO/Orphanet_254788

0 references

Identifiers

ICD-10-CM

G71.3

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

28 July 2018

0 references

mapping relation type

exact match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

28 July 2018

1 reference

inferred by common Orphanet mappings on source and on Wikidata

stated in

UMLS 2023

retrieved

16 June 2023

(Q55786434)

maternally-inherited mitochondrial myopathy

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