Meier-Gorlin syndrome 5

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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 Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: cdc6

MIM:

MIM:613805 - meier-gorlin syndrome 5; mgors5

MIM:613805 - meier-gorlin syndrome 5; mgors5

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal recessive disease (is_a), Meier-Gorlin syndrome (is_a)