periventricular nodular heterotopia

Summary

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,

Echinobase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: ermard

OMIM:

MIM:300049 - heterotopia, periventricular, x-linked dominant
MIM:608097 - periventricular heterotopia with microcephaly, autosomal recessive; arphm
MIM:615544 - periventricular nodular heterotopia 6; pvnh6

MIM:300049 - heterotopia, periventricular, x-linked dominant

MIM:608097 - periventricular heterotopia with microcephaly, autosomal recessive; arphm

MIM:615544 - periventricular nodular heterotopia 6; pvnh6

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): congenital nervous system abnormality (is_a)