(Q21124539)

English

chromosome 16p12.1 deletion syndrome, 520kb

Human disease

Fragile Site 16P12
CHROMOSOME 16p12.1 DELETION SYNDROME, 520-KB
chromosome 16p12.1 deletion syndrome, type 520kb
Fragile Site, Distamycin a Type, Rare, Fra(16)(P12.1)
Chromosome 16p12.1 Deletion 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

29 November 2021

Disease Ontology ID

on focus list of Wikimedia project

WikiProject Medicine

0 references

NCI Thesaurus ID

C129875

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

http://purl.obolibrary.org/obo/DOID_0060399

1 reference

Disease Ontology

29 November 2021

Disease Ontology ID

http://identifiers.org/doid/DOID:0060399

1 reference

Identifiers.org

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

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

29 November 2021

Disease Ontology ID

0 references

1 reference

Disease Ontology

28 August 2019

Disease Ontology ID

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

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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