(Q55790008)

English

chromosome 16p13.3 deletion syndrome

human disease

RSTS, Severe
Rubinstein-Taybi Syndrome, Severe

In more languages

default for all languages

No label defined

No description defined

Statements

developmental defect during embryogenesis

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

Rubinstein-Taybi syndrome

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

Identifiers

MeSH descriptor ID

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

ICD-11 ID (Foundation)

0 references

0 references

1 reference

based on heuristic

inferred by common MeSH mappings on source and on Wikidata

25 May 2023

Sitelinks

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Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

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