Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
DOID:0050454 - periventricular nodular heterotopia

Disease Ontology Definition:A congenital nervous system abnormality characterized by non proper migration of neurons during the early development of the fetal brain.

Synonyms: periventricular heterotopia

Xenbase Genes : nedd4l, arf1, ermard, tmtc3, arfgef2, map1b, flna

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0020341 - periventricular nodular heterotopia

MIM:
MIM:300049 - PERIVENTRICULAR NODULAR HETEROTOPIA 1; PVNH1
MIM:608097 - PERIVENTRICULAR HETEROTOPIA WITH MICROCEPHALY, AUTOSOMAL RECESSIVE; ARPHM
MIM:608098 - PERIVENTRICULAR NODULAR HETEROTOPIA 3; PVNH3
MIM:612881 - CHROMOSOME 5q14.3 DELETION SYNDROME, DISTAL
MIM:615544 - PERIVENTRICULAR NODULAR HETEROTOPIA 6; PVNH6

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): congenital nervous system abnormality (is_a)