(Q8067052)

English

myofibrillar myopathy 4

Human disease

zaspopathy
Late-onset distal myopathy, Markesbery-Griggs type
myofibrillar myopathy type 4
MYOPATHY, MYOFIBRILLAR, 4; MFM4
Myopathy, Myofibrillar, type 4
MFM4
ZASP-related myofibrillar myopathy
MYOPATHY, MYOFIBRILLAR, 4

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Statements

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myofibrillar myopathy

1 reference

30 November 2020

qualitative or quantitative defects of protein ZASP

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

retrieved

28 July 2018

Mondo ID

MONDO_0012277

autosomal dominant distal myopathy

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

retrieved

28 July 2018

Mondo ID

MONDO_0012277

autosomal dominant disease

1 reference

30 November 2020

2 references

13 August 2019

Mutations in ZASP define a novel form of muscular dystrophy in humans

on focus list of Wikimedia project

WikiProject Medicine

0 references

exact match

http://purl.obolibrary.org/obo/DOID_0080095

1 reference

30 November 2020

http://identifiers.org/doid/DOID:0080095

1 reference

stated in

Identifiers.org

reference URL

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

http://www.orpha.net/ORDO/Orphanet_98912

0 references

Identifiers

MeSH descriptor ID

C563718

mapping relation type

exact match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

28 July 2018

1 reference

30 November 2020

0 references

1 reference

Monarch Disease Ontology release 2018-06-29

retrieved

28 July 2018

Mondo ID

MONDO_0012277

Microsoft Academic ID

0 references

0 references

1 reference

28 August 2019

mapping relation type

exact match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

28 July 2018

mapping relation type

close match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

28 July 2018

0 references

Sitelinks

Wikipedia(1 entry)

enwiki Zaspopathy

(Q8067052)

myofibrillar myopathy 4

Statements

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Wikipedia(1 entry)

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