Periventricular Nodular Heterotopia Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
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)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D054091
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Genes

1 genes/proteins associated with the disease Periventricular Nodular Heterotopia from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
FLNA filamin A, alpha 2.88009