(Q55784758)

English

severe combined immunodeficiency due to IKK2 deficiency

human disease

Immunodeficiency type 15
IMMUNODEFICIENCY 15; IMD15
IMD15
IMMUNODEFICIENCY 15
SCID due to IKK2 deficiency

In more languages

Statements

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class of disease

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T+ B+ severe combined immunodeficiency

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

genetic association

2 references

Deficiency of innate and acquired immunity caused by an IKBKB mutation.

Open Targets Platform

24 August 2023

https://platform.opentargets.org/evidence/ENSG00000104365/MONDO_0014267

based on heuristic

inferred from an Open Targets association score over 0.7

http://www.orpha.net/ORDO/Orphanet_397787

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Identifiers

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

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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

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

1 reference

based on heuristic

inferred by common Orphanet mappings on source and on Wikidata

16 June 2023

Sitelinks

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