(Q23893414)

English

myofibrillar myopathy

myopathy that is characterized by slowly progressive muscle weakness that can involve both proximal muscles and distal muscles

Myofibrillar Myopathies
Myofibrillar myopathy

In more languages

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Statements

0 references

2 references

15 May 2019

30 November 2020

0 references

2 references

8 December 2020

https://search.clinicalgenome.org/kb/gene-validity/5466

25 January 2022

https://search.clinicalgenome.org/kb/gene-validity/CGGCIEX:assertion_5466

2 references

31 August 2020

https://search.clinicalgenome.org/kb/gene-validity/93dbca4d-5b8c-42f2-b8a3-41128b417dcb--2020-08-20T18:24:04

25 January 2022

https://search.clinicalgenome.org/kb/gene-validity/CGGV:assertion_93dbca4d-5b8c-42f2-b8a3-41128b417dcb-2020-08-20T182404.015Z

on focus list of Wikimedia project

WikiProject Medicine

0 references

ICD-9-CM

359.89

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

7 August 2018

C83009

0 references

C83009

mapping relation type

exact match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

7 August 2018

http://purl.obolibrary.org/obo/DOID_0080307

1 reference

30 November 2020

http://purl.obolibrary.org/obo/HP_0003715

1 reference

stated in

Human Phenotype Ontology release 2018-03-08

retrieved

8 October 2018

Human Phenotype Ontology ID

HP:0003715

http://www.orpha.net/ORDO/Orphanet_593

0 references

http://identifiers.org/doid/DOID:0080307

1 reference

stated in

Identifiers.org

reference URL

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

Identifiers

MeSH descriptor ID

C580316

mapping relation type

exact match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

7 August 2018

2 references

Human Phenotype Ontology release 2018-03-08

retrieved

8 October 2018

Human Phenotype Ontology ID

28 August 2019

0 references

1 reference

30 November 2020

1 reference

28 August 2019

Human Phenotype Ontology ID

HP:0003715

2 references

stated in

Monarch Disease Ontology release 2018-06-29

7 August 2018

Human Phenotype Ontology release 2018-03-08

retrieved

8 October 2018

Human Phenotype Ontology ID

0 references

1 reference

Monarch Disease Ontology release 2018-06-29

7 August 2018

0 references

8C76

Myofibrillar myopathy

0 references

Medical Dictionary for Regulatory Activities ID

10028300

1 reference

reference URL

https://cdn.who.int/media/docs/default-source/classification/icd/icd-10/icd-10-to-meddra-map---june-2023---codes-mapping.xlsx

based on heuristic

inferred by common ICD-10 mappings on Wikidata and on source

0 references

0 references

mapping relation type

exact match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

7 August 2018

mapping relation type

close match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

7 August 2018

1 reference

Human Phenotype Ontology release 2018-03-08

retrieved

8 October 2018

Human Phenotype Ontology ID

HP:0003715

Sitelinks

Wikipedia(1 entry)

dewiki Myofibrilläre Myopathie

(Q23893414)

myofibrillar myopathy

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Identifiers

Sitelinks

Wikipedia(1 entry)

Wikibooks(0 entries)

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Wikiquote(0 entries)

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Wikiversity(0 entries)

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Wiktionary(0 entries)

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