Meier-Gorlin syndrome 6 Disease Ontology Browser

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Disease Ontology Browser

Meier-Gorlin syndrome 6 (DOID:0080517)
Alliance: disease page
Alt IDs: OMIM:616835
Definition: A Meier-Gorlin syndrome that has_material_basis_in heterozygous mutation in the GMNN gene on chromosome 6p22.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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