OBO ID: DOID:0060364
Term Name: Galloway-Mowat syndrome 1 Search Ontology:
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. (2)
References:
Ontology: Human Disease   ( DOID:0060364 )
OTHER Galloway-Mowat syndrome 1 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
WDR73 Galloway-Mowat syndrome 1 251300
ZEBRAFISH MODELS
Fish Conditions Citations
WT + MO1-nup133 standard conditions Fujita et al., 2018
PHENOTYPE No data available

CITATIONS (4)