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Summary Literature (0)
MIM:608098 - PERIVENTRICULAR NODULAR HETEROTOPIA 3; PVNH3

Xenbase Genes:

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011967 - heterotopia, periventricular, associated with chromosome 5P anomalies
MONDO:0016292 - nodular neuronal heterotopia
MONDO:0020341 - periventricular nodular heterotopia

Disease Ontology (DO):
DOID:0050454 - periventricular nodular heterotopia