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Meier-Gorlin Syndrome 6

Disease ID: disease_node_20117

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DbxrefMIM:616835
SubclassofDOID_0050736, DOID_0060306
Data SourceDOID
Doid LabelMeier-Gorlin syndrome 6
Doid DescriptionA Meier-Gorlin syndrome that has_material_basis_in heterozygous mutation in the GMNN gene on chromosome 6p22.
Has Material Basis InGENO_0000147
Disease Node Iddisease_node_20117
Doid IdDOID_0080517
LabelMeier-Gorlin Syndrome 6