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Summary Literature (1)
DOID:0050577 - Sensenbrenner syndrome


Disease Ontology Definition:n_a

Synonyms: Levin syndrome, cranioectodermal dysplasia

Xenbase Genes : wdr19, ift122, ift52, wdr35, ift43

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0009032 - cranioectodermal dysplasia

OMIM:
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)