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Disease Ontology Browser
Galloway-Mowat syndrome 1 (DOID:0060364)
Alliance: disease page
Synonyms: autosomal recessive spinocerebellar ataxia 5; Galloway syndrome; microcephaly, hiatal hernia and nephrotic syndrome; nephrosis-microcephaly syndrome; nephrosis-neuronal dysmigration syndrome; SCAR5
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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12/10/2024
MGI 6.24 		The Jackson Laboratory