(Q26492828)

English

multiple mitochondrial dysfunctions syndrome 3

Human disease

MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 3
Multiple Mitochondrial Dysfunctions Syndrome type 3
MMDS3
MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 3; MMDS3
IBA57 deficiency

In more languages

Statements

0 references

class of disease

0 references

autosomal recessive disease

1 reference

Disease Ontology

15 May 2019

Disease Ontology ID

fatal multiple mitochondrial dysfunctions syndrome

1 reference

Disease Ontology

15 May 2019

Disease Ontology ID

genetic association

3 references

UniProt protein ID

13 August 2019

Mutation of the iron-sulfur cluster assembly gene IBA57 causes severe myopathy and encephalopathy

Open Targets Platform

24 August 2023

https://platform.opentargets.org/evidence/ENSG00000181873/MONDO_0014132

based on heuristic

inferred from an Open Targets association score over 0.7

on focus list of Wikimedia project

WikiProject Medicine

0 references

http://purl.obolibrary.org/obo/DOID_0080135

1 reference

Disease Ontology

15 May 2019

Disease Ontology ID

http://identifiers.org/doid/DOID:0080135

1 reference

Identifiers.org

http://www.ebi.ac.uk/miriam/main/collections/MIR:00000233

Identifiers

Disease Ontology ID

1 reference

Disease Ontology

15 May 2019

Disease Ontology ID

1 reference

Monarch Disease Ontology release 2018-06-29

7 August 2018

0 references

1 reference

Disease Ontology

15 May 2019

Disease Ontology ID

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

7 August 2018

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

7 August 2018

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

7 August 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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