syndromic intellectual disability autosomal recessive disease Galloway-Mowat syndrome DOID:0080694 GAMOS GARD:0000065 GARD:65 Galloway Mowat syndrome Galloway syndrome Galloway syndrome is characterized by the association of nephrotic syndrome and central nervous system anomalies. Galloway-Mowat syndrome ICD10:Q04.3 MESH:C537548 MONDO:0009627 NCIT:C132195 OMIMPS:251300 Orphanet:2065 SCTID:721297008 UMLS:C0795949 cerebellar ataxia with intellectual disability, optic atrophy, and skin abnormalities cerebellar ataxia with mental retardation, optic atrophy, and skin abnormalities hiatal hernia-microcephaly-nephrosis, Galloway type microcephaly nephrosis syndrome microcephaly, hiatal hernia and nephrotic syndrome microcephaly, hiatal hernia, and nephrotic syndrome microcephaly-hiatus hernia-nephrotic syndrome nephrosis neuronal dysmigration syndrome nephrosis-microcephaly syndrome nephrosis-neuronal dysmigration syndrome spinocerebellar ataxia, autosomal recessive 5 spinocerebellar ataxia, autosomal recessive 5, formerly primary glomerular disease other syndrome with a central nervous system malformation as major feature genetic nervous system disorder