(Q55782523)

English

immunodeficiency 50

human disease

Immunodeficiency type 50
Immunodeficiency 50
IMD50

In more languages

Statements

0 references

class of disease

0 references

genetic disease

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

primary immunodeficiency disease

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

X-linked recessive disease

1 reference

Disease Ontology

30 November 2020

Disease Ontology ID

combined immunodeficiency

1 reference

Disease Ontology

18 January 2022

Disease Ontology ID

genetic association

1 reference

X-linked primary immunodeficiency associated with hemizygous mutations in the moesin (MSN) gene

http://purl.obolibrary.org/obo/DOID_0112001

1 reference

Disease Ontology

18 January 2022

Disease Ontology ID

http://identifiers.org/doid/DOID:0112001

1 reference

Identifiers.org

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

Identifiers

Disease Ontology ID

1 reference

Disease Ontology

18 January 2022

Disease Ontology ID

0 references

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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