(Q4633988)

English

2p15-16.1 microdeletion syndrome

Human disease

chromosome 2p16.1-p15 deletion syndrome
2p15p16.1 microdeletion syndrome
2p15-p16.1 microdeletion syndrome
CHROMOSOME 2p16.1-p15 DELETION SYNDROME
Del(2)(p15p16.1)
Monosomy 2p15p16.1
Monosomy 2p15-p16.1

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Statements

instance of

developmental defect during embryogenesis

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

28 July 2018

0 references

chromosomal deletion syndrome

1 reference

15 May 2019

partial deletion of the short arm of chromosome 2

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

28 July 2018

0 references

on focus list of Wikimedia project

WikiProject Medicine

0 references

exact match

http://purl.obolibrary.org/obo/DOID_0060415

1 reference

28 August 2019

http://identifiers.org/doid/DOID:0060415

1 reference

stated in

Identifiers.org

reference URL

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

http://www.orpha.net/ORDO/Orphanet_261349

0 references

Identifiers

MeSH descriptor ID

C567289

mapping relation type

exact match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

28 July 2018

1 reference

28 August 2019

1 reference

28 August 2019

2 references

28 August 2019

Monarch Disease Ontology release 2018-06-29

28 July 2018

0 references

Microsoft Academic ID

0 references

0 references

1 reference

28 August 2019

1 reference

28 August 2019

mapping relation type

close match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

28 July 2018

1 reference

inferred by common Orphanet mappings on source and on Wikidata

stated in

UMLS 2023

retrieved

16 June 2023

(Q4633988)

2p15-16.1 microdeletion syndrome

Statements

Identifiers

Sitelinks

Wikipedia(3 entries)

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