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Galloway-Mowat Syndrome 4

Disease ID: disease_node_20285

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DbxrefMIM:617730
SubclassofDOID_0050737, DOID_0080694
Data SourceDOID
Doid LabelGalloway-Mowat syndrome 4
Doid DescriptionA Galloway-Mowat syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the TP53RK gene on chromosome 20q13.
Has Material Basis InGENO_0000148
Disease Node Iddisease_node_20285
Doid IdDOID_0080246
LabelGalloway-Mowat Syndrome 4