Term Name:	Galloway-Mowat syndrome 1
Synonyms:	autosomal recessive spinocerebellar ataxia 5, Galloway syndrome, microcephaly, hiatal hernia and nephrotic syndrome, nephrosis-microcephaly syndrome, nephrosis-neuronal dysmigration syndrome, SCAR5
Definition:	A Galloway-Mowat syndrome that has_material_basis_in homozygous mutation in the WDR73 gene on chromosome 15q25.
Ontology:	Human Disease [DOID:0060364]   ( DOID:0060364 )