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Summary Literature (0)
DOID:0050577 - Sensenbrenner syndrome

Disease Ontology Definition:n_a

Synonyms: Levin syndrome, cranioectodermal dysplasia,

Echinobase Genes : ift122, wdr35

OMIM:218330 - cranioectodermal dysplasia 1; ced1
OMIM:613610 - cranioectodermal dysplasia 2; ced2

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

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