(Q32139991)

English

congenital myasthenic syndrome 3A

human disease

CMS3A
congenital myasthenic syndrome 3A, slow-channel
MYASTHENIC SYNDROME, CONGENITAL, 3A, SLOW-CHANNEL
congenital myasthenic syndrome type 3A
MYASTHENIC SYNDROME, CONGENITAL, 3A, SLOW-CHANNEL; CMS3A

In more languages

Statements

0 references

class of disease

0 references

congenital myasthenic syndrome

1 reference

Disease Ontology

15 May 2019

Disease Ontology ID

postsynaptic congenital myasthenic syndrome

1 reference

Monarch Disease Ontology release 2018-06-29

7 August 2018

genetic disease

1 reference

Disease Ontology

15 May 2019

Disease Ontology ID

genetic association

2 references

UniProt protein ID

13 August 2019

Novel delta subunit mutation in slow-channel syndrome causes severe weakness by novel mechanisms

on focus list of Wikimedia project

WikiProject Medicine

0 references

http://purl.obolibrary.org/obo/DOID_0110666

1 reference

Disease Ontology

28 August 2019

Disease Ontology ID

http://identifiers.org/doid/DOID:0110666

1 reference

Identifiers.org

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

Identifiers

Disease Ontology ID

1 reference

Disease Ontology

28 August 2019

Disease Ontology ID

0 references

1 reference

Disease Ontology

28 August 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

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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