FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term bilateral parasagittal parieto-occipital polymicrogyria ID (Ontology) DOID:0080923 (Human Disease)
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.
Also Known As "bilateral temporooccipital polymicrogyria"
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 Genes
 bilateral parasagittal parieto-occipital polymicrogyria       1
 for disease ribbon | bilateral parasagittal parieto-occipital polymicrogyria       1
 model of | bilateral parasagittal parieto-occipital polymicrogyria       1
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal recessive disease__
brain disease                    |
 |__polymicrogyria_______________|
                                 bilateral parasagittal parieto-occipital polymicrogyria  1 rec.
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Is a autosomal recessive disease
polymicrogyria
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Synonyms
  • "bilateral temporooccipital polymicrogyria" EXACT
Secondary IDs
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GARD:10785
MIM:612691
ORDO:208441