(Q55781980)

(Redirected from Q102293947)

English

hypoproteinemia, Hypercatabolic

human disease

HYPOPROTEINEMIA, HYPERCATABOLIC
immunodeficiency 43
IMD43
B2M deficiency
hypercatabolic hypoproteinemia
beta-2-microglobulin deficiency

In more languages

Statements

0 references

class of disease

0 references

hypoproteinemia

0 references

autosomal recessive disease

1 reference

Disease Ontology

29 November 2020

Disease Ontology ID

primary immunodeficiency disease

1 reference

Disease Ontology

29 November 2020

Disease Ontology ID

genetic association

1 reference

Familial hypercatabolic hypoproteinemia caused by deficiency of the neonatal Fc receptor, FcRn, due to a mutant beta2-microglobulin gene

http://purl.obolibrary.org/obo/DOID_0111981

1 reference

Disease Ontology

29 November 2020

Disease Ontology ID

http://identifiers.org/doid/DOID:0111981

1 reference

Identifiers.org

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

Identifiers

MeSH descriptor ID

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

0 references

Disease Ontology ID

1 reference

Disease Ontology

29 November 2020

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)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q55781980&oldid=2087364720"