Disease Details | GeDiPNet - Gene Disease Associations & Pathways

Disease Term	Disease ID	Gene Symbol	Classification	References	Source
PERIVENTRICULAR HETEROTOPIA WITH MICROCEPHALY, AUTOSOMAL RECESSIVE	608097 MONDO:0011966	ARFGEF2	Causal	14647276 16320251 19384555 23755938 23812912 25160555 26126837	ClinGen ClinVar Disgenet HPO

Periventricular heterotopia with microcephaly, autosomal recessive