(Q55785141)

English

Sotos syndrome 3

human disease

Sotos Syndrome 3
Sotos Syndrome type 3
SOTOS3

In more languages

Statements

developmental defect during embryogenesis

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

0 references

class of disease

0 references

1 reference

Disease Ontology

23 November 2020

Disease Ontology ID

autosomal recessive disease

1 reference

Disease Ontology

23 November 2020

Disease Ontology ID

genetic association

2 references

UniProt protein ID

13 August 2019

Loss-of-Function Mutation in APC2 Causes Sotos Syndrome Features

http://purl.obolibrary.org/obo/DOID_0112104

1 reference

Disease Ontology

23 November 2020

Disease Ontology ID

http://identifiers.org/doid/DOID:0112104

1 reference

Identifiers.org

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

Identifiers

Disease Ontology ID

1 reference

Disease Ontology

23 November 2020

Disease Ontology ID

0 references

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

UniProt disease ID

0 references

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)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q55785141&oldid=2087987251"