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Summary Literature (0)
DOID:0112369 - Coffin-Siris syndrome 7

Disease Ontology Definition:A Coffin-Siris syndrome characterized by global developmental delay with mild to moderate intellectual disability, speech impairment, behavioral abnormalities, poor overall growth, coarse facial features, and hypoplastic fifth toenails that has_material_basis_in heterozygous mutation in the DPF2 gene on chromosome 11q13.1.

Synonyms: CSS7,

Xenbase Genes : dpf2



Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): Coffin-Siris syndrome (is_a)