|OBO ID: DOID:0060364|
|Term Name:||Galloway-Mowat syndrome 1||Search Ontology:|
|Definition:||A Galloway-Mowat syndrome that has_material_basis_in homozygous mutation in the WDR73 gene on chromosome 15q25. (2)|
|Ontology:||Human Disease (DOID:0060364)|
|is a type of:||
OTHER Galloway-Mowat syndrome 1 PAGES
PHENOTYPE No data available
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