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Disease Ontology Browser
Galloway-Mowat syndrome 1 (DOID:0060364)
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Synonyms: Galloway syndrome; microcephaly, hiatal hernia and nephrotic syndrome; nephrosis-microcephaly syndrome; nephrosis-neuronal dysmigration syndrome
Alt IDs: OMIM:251300
Definition: A Galloway-Mowat syndrome that has_material_basis_in homozygous mutation in the WDR73 gene on chromosome 15q25.


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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last database update
06/15/2021
MGI 6.17
The Jackson Laboratory