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Summary Literature (1)
DOID:0070120 - Meckel syndrome 6

Disease Ontology Definition:A Meckel syndrome that has_material_basis_in an autosomal recessive mutation of the CC2D2A gene on chromosome 4p15.32.

Synonyms: MKS6, Meckel-Gruber syndrome, type 6,

Xenbase Genes : cc2d2a

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012848 - Meckel syndrome, type 6

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

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