(Q21154057)

English

chromosome 15q11.2 deletion syndrome

human disease

15q11.2 microdeletion syndrome
CHROMOSOME 15q11.2 DELETION SYNDROME
Del(15)(q11.2)
Monosomy 15q11.2
Burnside-Butler syndrome

In more languages

Statements

developmental defect during embryogenesis

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

class of disease

0 references

chromosomal deletion syndrome

1 reference

Disease Ontology

15 May 2019

Disease Ontology ID

Chromosome 15q partial deletion

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

on focus list of Wikimedia project

WikiProject Medicine

0 references

http://purl.obolibrary.org/obo/DOID_0060393

2 references

Disease Ontology

28 August 2019

Disease Ontology ID

Disease Ontology

10 July 2020

Disease Ontology ID

http://identifiers.org/doid/DOID:0060393

2 references

Identifiers.org

http://www.ebi.ac.uk/miriam/main/collections/MIR:00000233

Disease Ontology

10 July 2020

Disease Ontology ID

http://www.orpha.net/ORDO/Orphanet_261183

0 references

Identifiers

MeSH descriptor ID

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

Disease Ontology ID

1 reference

Disease Ontology

10 July 2020

Disease Ontology ID

GARD rare disease ID

1 reference

Genetic and Rare Diseases Information Center

29 March 2019

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

Microsoft Academic ID

0 references

0 references

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

Sitelinks

Wikipedia(1 entry)

enwiki Burnside–Butler syndrome

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)

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