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Summary Literature (0)
DOID:0061009 - craniosynostosis 2

Disease Ontology Definition:A craniosynostosis characterized by a highly variable craniosynostosis with frontal bossing, turribrachycephaly and cloverleaf skull anomaly that has_material_basis_in heterozygous mutation in the MSX2 gene on chromosome 5q35.

Synonyms: Craniosynostosis Boston type, Craniosynostosis Warman type, CRS2, Warman-Mulliken-Hayward syndrome

Xenbase Genes :



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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal dominant disease (is_a), craniosynostosis (is_a)