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Microcephaly And Chorioretinopathy 2

Disease ID: disease_node_20315

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DbxrefMIM:616171
SubclassofDOID_225, DOID_0050737
Data SourceDOID
Doid Labelmicrocephaly and chorioretinopathy 2
Doid DescriptionA syndrome that is characterized by delayed psychomotor development, visual impairment, and short stature and has_material_basis_in homozygous mutation in the PLK4 gene.
Has Material Basis InGENO_0000148
Disease Node Iddisease_node_20315
Doid IdDOID_0080106
LabelMicrocephaly And Chorioretinopathy 2