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Summary Literature (0)
MIM:608097 - PERIVENTRICULAR HETEROTOPIA WITH MICROCEPHALY, AUTOSOMAL RECESSIVE; ARPHM

Xenbase Genes: arfgef2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011966 - periventricular heterotopia with microcephaly, autosomal recessive
MONDO:0016292 - nodular neuronal heterotopia
MONDO:0020341 - periventricular nodular heterotopia

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