| 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 |
| Similar Terms | |
| Downloads & Tools |
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 |
