Galloway-Mowat syndrome 10 Disease Ontology Browser

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Disease Ontology Browser

Galloway-Mowat syndrome 10 (DOID:0061293)
Alliance: disease page
Alt IDs: OMIM:619609
Definition: A Galloway-Mowat syndrome characterized by onset of symptoms soon after birth that has_material_basis_in homozygous or compound heterozygous mutation in the YRDC gene on chromosome 1p34.

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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