|Dataset||OMIM Gene-Disease Associations|
|Category||disease or phenotype associations|
|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)|
|Downloads & Tools|
3 genes associated with the neural tube defects phenotype from the curated OMIM Gene-Disease Associations dataset.