neural tube defects Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of or development of the hollow epithelial tube found on the dorsal side of the vertebrate embryo that develops into the central nervous system (i.e. brain and spinal cord) (Mammalian Phenotype Ontology, MP_0002151)
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3 genes associated with the neural tube defects phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
FUZ fuzzy planar cell polarity protein
VANGL1 VANGL planar cell polarity protein 1
VANGL2 VANGL planar cell polarity protein 2