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Echinobase
Summary Literature (0)
DOID:0050778 - Meckel syndrome

Disease Ontology Definition:A ciliopathy that is characterized by renal cystic dysplasia, occipital encephalocele, polydactyly (post axial), hepatic developmental defects, and pulmonary hypoplasia.

Synonyms: Meckel-Gruber syndrome,

Echinobase Genes : cep290, mks1, tmem67



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

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