(Q66299850)

English

congenital disorder of glycosylation It

human disease

congenital disorder of glycosylation 1t
glycogen storage disease type 14
Congenital disorder of glycosylation type 1t
Phosphoglucomutase-1 deficiency
PGM1-CDG

In more languages

Statements

0 references

class of disease

0 references

congenital disorder of glycosylation type I

0 references

glycogen storage disease

0 references

genetic association

1 reference

Muscle glycogenosis due to phosphoglucomutase 1 deficiency

on focus list of Wikimedia project

WikiProject Medicine

0 references

http://purl.obolibrary.org/obo/DOID_0080570

1 reference

Disease Ontology

28 August 2019

Disease Ontology ID

Identifiers

MeSH descriptor ID

0 references

1 reference

https://www.kegg.jp/entry/H01954

Disease Ontology ID

1 reference

Disease Ontology

28 August 2019

Disease Ontology ID

GARD rare disease ID

0 references

ICD-11 (foundation)

0 references

1 reference

Disease Ontology

28 August 2019

Disease Ontology ID

1 reference

Disease Ontology

28 August 2019

Disease Ontology ID

1 reference

based on heuristic

inferred by common MeSH mappings on source and on Wikidata

25 May 2023

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=Q66299850&oldid=1982358159"