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Echinobase
Summary Literature (0)
DOID:0080516 - Meier-Gorlin syndrome 5

Disease Ontology Definition:A Meier-Gorlin syndrome that has_material_basis_in homozygous mutation in the CDC6 gene on chromosome 17q21.

Synonyms:

Echinobase Genes : cdc6


OMIM:
MIM:613805 - meier-gorlin syndrome 5; mgors5

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

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