(Q21505523)

English

myofibrillar myopathy 5

Human disease

filaminopathy
Filaminopathy, Autosomal Dominant
MFM5
MYOPATHY, MYOFIBRILLAR, 5
Muscle filaminopathy
Myopathy, Myofibrillar, type 5
myofibrillar myopathy type 5
MYOPATHY, MYOFIBRILLAR, 5; MFM5
Myopathy, Myofibrillar, Filamin C-Related

In more languages

Statements

0 references

class of disease

0 references

myofibrillar myopathy

1 reference

Disease Ontology

27 November 2020

Disease Ontology ID

qualitative or quantitative defects of filamin c

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

autosomal dominant disease

1 reference

Disease Ontology

27 November 2020

Disease Ontology ID

genetic association

5 references

on focus list of Wikimedia project

WikiProject Medicine

0 references

http://purl.obolibrary.org/obo/DOID_0080096

1 reference

Disease Ontology

27 November 2020

Disease Ontology ID

http://identifiers.org/doid/DOID:0080096

1 reference

Identifiers.org

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

http://www.orpha.net/ORDO/Orphanet_171445

0 references

Identifiers

MeSH descriptor ID

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

Disease Ontology ID

1 reference

Disease Ontology

27 November 2020

Disease Ontology ID

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

0 references

1 reference

Disease Ontology

28 August 2019

Disease Ontology ID

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

UniProt disease ID

0 references

Sitelinks

Wikipedia(0 entries)

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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