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 3 ID (Ontology) DOID:0080245 (Human Disease)
Definition A Galloway-Mowat syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the OSGEP gene on chromosome 14q11.
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Data Class Field Records
Alleles (FBal)  HUMAN_DISEASE_INTERACTIONS      10
Human Disease Models (FBhh)  DOID       1
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 Alleles Genes Human Disease Models
 Galloway-Mowat syndrome 3      10      4      1
 ameliorates | Galloway-Mowat syndrome 3       3       --       --
 exacerbates | Galloway-Mowat syndrome 3       1       --       --
 for disease ribbon | Galloway-Mowat syndrome 3       --       1       --
 model of | Galloway-Mowat syndrome 3       6      1       --
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal recessive disease__
syndrome                         |
 |__Galloway-Mowat syndrome______|
                                 Galloway-Mowat syndrome 3  15 rec.
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Is a autosomal recessive disease
Galloway-Mowat syndrome
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MIM:617729