Galloway-Mowat syndrome 5 Disease Ontology Browser

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Disease Ontology Browser

Galloway-Mowat syndrome 5 (DOID:0080247)
Alliance: disease page
Alt IDs: OMIM:617731
Definition: A Galloway-Mowat syndrome that has_material_basis_in homozygous mutation in the TPRKB gene on chromosome 2p13.

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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