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Summary Literature (0)
DOID:0080508 - Cornelia de Lange syndrome 4


Disease Ontology Definition:A Cornelia de Lange syndrome that has_material_basis_in heterozygous mutation in the RAD21 gene, which encodes a component of the cohesin complex, on chromosome 8q24.

Synonyms: CDLS4, Cornelia De Lange syndrome 4 with or without midline brain defects

In OMIM:
OMIM:614701 - CORNELIA DE LANGE SYNDROME 4 WITH OR WITHOUT MIDLINE BRAIN DEFECTS; CDLS4


Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : rad21

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): Cornelia de Lange syndrome (is_a), autosomal dominant disease (is_a)