DISEASES

Disease-gene associations mined from literature

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Human genes for Carey-Fineman-Ziter syndrome

Carey-Fineman-Ziter syndrome [DOID:0080194]

A 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.

Synonyms:  Carey-Fineman-Ziter syndrome,  CareyFinemanZiter syndrome,  Carey-Fineman-Ziter disease,  Carey-Fineman-Ziter disorder,  Carey-Fineman-Ziter syndromes ...

The disease-gene associations are derived from automatic text mining of the biomedical literature, manually curated database annotations, cancer mutation data, and genome-wide association studies. The confidence of each association is signified by stars, where ★★★★★ is the highest confidence and ★☆☆☆☆ is the lowest.

Developed by Sune Frankild, Alexander Junge, Albert Pallejà, Dhouha Grissa, Kalliopi Tsafou, and Lars Juhl Jensen from the Novo Nordisk Foundation Center for Protein Research.