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Carey-Fineman-Ziter Syndrome

Disease ID: disease_node_20301

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DbxrefMIM:254940
SubclassofDOID_225
Data SourceDOID
Doid LabelCarey-Fineman-Ziter syndrome
Doid DescriptionA syndrome characterized by hypotonia, Moebius sequence (bilateral congenital facial palsy with impairment of ocular abduction), Pierre Robin complex (micrognathia, glossoptosis, and high-arched or cleft palate), delayed motor milestones, and failure to thrive.
Has SymptomSYMP_0000369
Disease Node Iddisease_node_20301
Doid IdDOID_0080194
LabelCarey-Fineman-Ziter Syndrome