Catel Manzke syndrome Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Catel-Manzke syndrome is a rare bone disease characterized by bilateral hyperphalangy and clinodactyly of the index finger typically in association with Pierre Robin sequence (see this term) comprising micrognathia, cleft palate and glossoptosis. (Orphanet Rare Disease Ontology, Orphanet_1388)
External Link http://www.omim.org/entry/616145
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Genes

1 genes associated with the Catel Manzke syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
TGDS TDP-glucose 4,6-dehydratase