FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
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General Information
Term Galloway-Mowat syndrome 4 ID (Ontology) DOID:0080246 (Human Disease)
Definition A Galloway-Mowat syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the TP53RK gene on chromosome 20q13.
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 Genes
 Galloway-Mowat syndrome 4       1
 for disease ribbon | Galloway-Mowat syndrome 4       1
 model of | Galloway-Mowat syndrome 4       1
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal recessive disease__
syndrome                         |
 |__Galloway-Mowat syndrome______|
                                 Galloway-Mowat syndrome 4  1 rec.
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Is a autosomal recessive disease
Galloway-Mowat syndrome
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MIM:617730