(Q55788992)

English

maternal uniparental disomy of chromosome 20

human disease

Maternal UPD(20)
Maternal uniparental disomy of chromosome type 20
UPD(20)mat
Mulchandani-Bhoj-Conlin 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

uniparental disomy of maternal origin

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

1 reference

Disease Ontology

27 November 2020

Disease Ontology ID

http://www.orpha.net/ORDO/Orphanet_96186

0 references

http://purl.obolibrary.org/obo/DOID_0111714

1 reference

Disease Ontology

27 November 2020

Disease Ontology ID

http://identifiers.org/doid/DOID:0111714

1 reference

Identifiers.org

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

Identifiers

Disease Ontology ID

1 reference

Disease Ontology

27 November 2020

Disease Ontology ID

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

ICD-11 (foundation)

0 references

0 references

mapping relation type

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

1 reference

based on heuristic

inferred by common Orphanet mappings on source and on Wikidata

16 June 2023

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)

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