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Summary Literature (0)
DOID:0111705 - oculoectodermal syndrome

Disease Ontology Definition:An ectodermal dysplasia characterized by epibulbar dermoids and aplasia cutis congenita that has_material_basis_in somatic mosaic mutation in the KRAS gene on chromosome 12p12.1.

Synonyms: Toriello-Lacassie-Droste syndrome, aplasia cutis congenita-epibulbar dermoids syndrome,

Xenbase Genes :



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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): ectodermal dysplasia (is_a)