cervical segmentation defect Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality related to a defect of vertebral separation of cervical vetebrae during development. (Human Phenotype Ontology, HP_0004632)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0004632
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Genes

1 genes associated with the cervical segmentation defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
FLNB filamin B, beta