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congenital heart defects, dysmorphic facial features, and intellectual developmental disorder (DOID:0112247)
Alliance: disease page
Synonyms: CDK13-Related CHDFIDD; CDK13-Related Disorder; CHDFIDD
Alt IDs: OMIM:617360
Definition: A syndrome characterized by congenital heart defects, dysmorphic facial features, and impaired intellectual developmental that has_material_basis_in heterozygous mutation in the CDK13 gene on chromosome 7p14.1.

Disease References using Mouse Models (1)
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory