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Galloway-Mowat Syndrome 3

Disease ID: disease_node_20286

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DbxrefMIM:617729
SubclassofDOID_0050737, DOID_0080694
Data SourceDOID
Doid LabelGalloway-Mowat syndrome 3
Doid DescriptionA Galloway-Mowat syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the OSGEP gene on chromosome 14q11.
Has Material Basis InGENO_0000148
Disease Node Iddisease_node_20286
Doid IdDOID_0080245
LabelGalloway-Mowat Syndrome 3