FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term Galloway-Mowat syndrome 1 ID (Ontology) DOID:0060364 (Human Disease)
Definition A Galloway-Mowat syndrome that has_material_basis_in homozygous mutation in the WDR73 gene on chromosome 15q25.
Also Known As "autosomal recessive spinocerebellar ataxia 5" ; "Galloway syndrome" ; "microcephaly, hiatal hernia and nephrotic syndrome" (for all, see Synonyms field below)
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autosomal genetic disease
 |__autosomal recessive disease__
syndrome                         |
 |__Galloway-Mowat syndrome______|
                                 Galloway-Mowat syndrome 1
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Is a autosomal recessive disease
Galloway-Mowat syndrome
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Synonyms
  • "autosomal recessive spinocerebellar ataxia 5" EXACT
    "Galloway syndrome" EXACT
    "microcephaly, hiatal hernia and nephrotic syndrome" EXACT
    "nephrosis-microcephaly syndrome" EXACT
    "nephrosis-neuronal dysmigration syndrome" EXACT
    "SCAR5" EXACT OMO:0003012
Secondary IDs
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MIM:251300