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.