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Summary Literature (0)
DOID:0080923 - bilateral parasagittal parieto-occipital polymicrogyria

Disease Ontology Definition:A polymicrogyria that is characterized by bilateral malformation of cortical development, centered around the parasagittal and mesial aspects of the parietooccipital cortex and that has_material_basis_in homozygous mutation in the FIG4 gene on chromosome 6q21.

Synonyms: bilateral temporooccipital polymicrogyria

Xenbase Genes : fig4


MIM:
MIM:612691 - POLYMICROGYRIA, BILATERAL TEMPOROOCCIPITAL; BTOP

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal recessive disease (is_a), polymicrogyria (is_a)