(Q21154066)

English

chromosome 19q13.11 deletion syndrome

Human disease

19q13.11 microdeletion syndrome
monosomy 19q13.11
CHROMOSOME 19q13.11 DELETION SYNDROME
Del(19)(q13.11)

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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

30 November 2020

multiple congenital anomalies/dysmorphic syndrome-intellectual disability

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

retrieved

28 July 2018

Mondo ID

MONDO_0013090

partial deletion of the long arm of chromosome 19

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

retrieved

28 July 2018

Mondo ID

MONDO_0013090

genetic syndromic intellectual disability

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

retrieved

28 July 2018

Mondo ID

MONDO_0013090

autosomal dominant disease

1 reference

30 November 2020

on focus list of Wikimedia project

WikiProject Medicine

0 references

exact match

http://purl.obolibrary.org/obo/DOID_0060408

1 reference

30 November 2020

http://identifiers.org/doid/DOID:0060408

1 reference

stated in

Identifiers.org

reference URL

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

http://www.orpha.net/ORDO/Orphanet_217346

0 references

Identifiers

MeSH descriptor ID

C567810

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

30 November 2020

2 references

Monarch Disease Ontology release 2018-06-29

28 July 2018

28 August 2019

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

0 references

0 references

1 reference

28 August 2019

1 reference

28 August 2019

1 reference

28 August 2019

1 reference

inferred by common Orphanet mappings on source and on Wikidata

stated in

UMLS 2023

retrieved

16 June 2023

Sitelinks

Wikipedia(1 entry)

trwiki 19q13.11 delesyonu sendromu

(Q21154066)

chromosome 19q13.11 deletion syndrome

Statements

Identifiers

Sitelinks

Wikipedia(1 entry)

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Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

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