(Q8020956)

English

Williams-Campbell syndrome

human disease

Williams-Campbell Syndrome
BRONCHOMALACIA

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

0 references

rare genetic developmental defect during embryogenesis

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

rare genetic respiratory disease

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

respiratory or mediastinal malformation

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

respiratory system abnormality

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

748.3

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

http://www.orpha.net/ORDO/Orphanet_411501

0 references

Identifiers

PatientsLikeMe condition ID

0 references

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

Microsoft Academic ID

0 references

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

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(4 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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