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Fraser Syndrome 3

Disease ID: disease_node_20263

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DbxrefMIM:617667
SubclassofDOID_0090001
Data SourceDOID
SynonymsFRASRS3
Doid LabelFraser syndrome 3
Doid DescriptionA Fraser syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the GRIP1 gene on chromosome 12q14.3.
Disease Node Iddisease_node_20263
Doid IdDOID_0111406
LabelFraser Syndrome 3