(Q69642903)

English

Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder

rare genetic disorder

CDK13-related disorder
CHDFIDD
Congenital heart defects, dysmorphic facial features and intellectual developmental disorder

In more languages

Statements

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Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing.

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Gene-Rare Disease-Provenance dataset collection

congenital heart disease

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health specialty

medical genetics

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genetic association

1 reference

Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing.

Commons category

CDK13-related disorder

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Identifiers

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Google Knowledge Graph ID

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1 reference

Online Mendelian Inheritance in Man

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UniProt disease ID

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Sitelinks

Wikipedia(4 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

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Wiktionary(0 entries)

Multilingual sites(1 entry)

commonswiki Category:CDK13-related disorder

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