Galloway-Mowat syndrome (Q4357083)

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autosomal recessive disease characterized by is a rare autosomal recessive disease, characterized by microcephaly with brain anomalies including CA in some cases, intellectual disability, and early-infantile-onset nephrotic syndrome
  • Galloway syndrome
  • microcephaly, hiatal hernia and nephrotic syndrome
  • nephrosis-microcephaly syndrome
  • nephrosis-neuronal dysmigration syndrome
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English
Galloway-Mowat syndrome
autosomal recessive disease characterized by is a rare autosomal recessive disease, characterized by microcephaly with brain anomalies including CA in some cases, intellectual disability, and early-infantile-onset nephrotic syndrome
  • Galloway syndrome
  • microcephaly, hiatal hernia and nephrotic syndrome
  • nephrosis-microcephaly syndrome
  • nephrosis-neuronal dysmigration syndrome

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