|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A congenital nervous system abnormality characterized by non proper migration of neurons during the early development of the fetal brain. (Human Disease Ontology, DOID_0050454)|
|Downloads & Tools|
1 genes/proteins associated with the disease Periventricular Nodular Heterotopia from the curated CTD Gene-Disease Associations dataset.
|FLNA||filamin A, alpha||2.88009|