Meier-Gorlin syndrome 6

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Summary

Literature (0)

DOID:0080517 - Meier-Gorlin syndrome 6

Disease Ontology Definition:A Meier-Gorlin syndrome that has_material_basis_in heterozygous mutation in the GMNN gene on chromosome 6p22.

Synonyms:

Xenbase 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

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

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

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