(Q55783887)

English

primary CD59 deficiency

human disease

HACD59
Cd59 Deficiency
HEMOLYTIC ANEMIA, CD59-MEDIATED, WITH OR WITHOUT IMMUNE-MEDIATED POLYNEUROPATHY
HEMOLYTIC ANEMIA, CD59-MEDIATED, WITH OR WITHOUT IMMUNE-MEDIATED POLYNEUROPATHY; HACD59

In more languages

Statements

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class of disease

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immunodeficiency due to a complement regulatory deficiency

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

genetic peripheral neuropathy

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

hereditary haemolytic anaemia due to red cell membrane defects

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

genetic association

2 references

Paroxysmal nocturnal hemoglobinuria due to hereditary nucleotide deletion in the HRF20 (CD59) gene

Open Targets Platform

24 August 2023

https://platform.opentargets.org/evidence/ENSG00000085063/MONDO_0012858

based on heuristic

inferred from an Open Targets association score over 0.7

http://www.orpha.net/ORDO/Orphanet_169464

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Identifiers

MeSH descriptor ID

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

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

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

UniProt disease ID

0 references

Sitelinks

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