(Q966149)

English

McLeod syndrome

rare disease

McLeod neuroacanthocytosis syndrome
Mcleod Phenotype
MLS
Neuroacanthocytosis, Mcleod Type
Mcleod Syndrome With Chronic Granulomatous Disease
MCLEOD SYNDROME
X-linked McLeod syndrome
MCLDS
MCLEOD SYNDROME; MCLDS

In more languages

default for all languages

No label defined

No description defined

Statements

designated intractable/rare disease

1 reference

https://ddrare.nibiohn.go.jp/

17 May 2019

0 references

class of disease

0 references

neuroacanthocytosis

2 references

Monarch Disease Ontology release 2018-06-29

3 July 2018

Disease Ontology

29 November 2020

Disease Ontology ID

nervous system heredodegenerative disease

1 reference

Monarch Disease Ontology release 2018-06-29

3 July 2018

rare genetic epilepsy

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

neurometabolic disease

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

constitutional hemolytic anemia due to acanthocytosis

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

syndrome associated with dilated cardiomyopathy

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

other metabolic disease with epilepsy

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

X-linked disease

1 reference

Disease Ontology

29 November 2020

Disease Ontology ID

genetic association

3 references

UniProt protein ID

13 August 2019

Isolation of the gene for McLeod syndrome that encodes a novel membrane transport protein

Open _targets Platform

24 August 2023

https://platform.open_targets.org/evidence/ENSG00000047597/MONDO_0018945

based on heuristic

inferred from an Open _targets association score over 0.7

external data available at URL

http://www.nanbyou.or.jp/entry/4051

language of work or name

1 reference

https://ddrare.nibiohn.go.jp/

17 May 2019

289.89

1 reference

Monarch Disease Ontology release 2018-06-29

3 July 2018

http://www.orpha.net/ORDO/Orphanet_59306

0 references

http://purl.obolibrary.org/obo/DOID_0112107

1 reference

Disease Ontology

29 November 2020

Disease Ontology ID

http://identifiers.org/doid/DOID:0112107

1 reference

Identifiers.org

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

Swyer-James syndrome

1 reference

Swyer-James syndrome

Identifiers

MeSH descriptor ID

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

3 July 2018

0 references

Disease Ontology ID

1 reference

Disease Ontology

29 November 2020

Disease Ontology ID

1 reference

imported from Wikimedia project

English Wikipedia

Encyclopædia Britannica Online ID

topic/McLeod-syndrome

subject named as

McLeod syndrome

0 references

1 reference

Freebase Data Dumps

publication date

28 October 2013

GARD rare disease ID

1 reference

Monarch Disease Ontology release 2018-06-29

3 July 2018

1 reference

imported from Wikimedia project

English Wikipedia

1 reference

Monarch Disease Ontology release 2018-06-29

3 July 2018

Microsoft Academic ID

0 references

0 references

mapping relation type

2 references

imported from Wikimedia project

English Wikipedia

Monarch Disease Ontology release 2018-06-29

3 July 2018

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

3 July 2018

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

3 July 2018

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

3 July 2018

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

3 July 2018

1 reference

based on heuristic

inferred by common Orphanet mappings on source and on Wikidata

16 June 2023

UniProt disease ID

0 references

WikiProjectMed ID

McLeod syndrome

0 references

Sitelinks

Wikipedia(12 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=Q966149&oldid=2286775440"

NODES