bilateral parasagittal parieto-occipital polymicrogyria

Summary
Synonym
  • bilateral temporooccipital polymicrogyria
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.
Super Class
autosomal recessive disease polymicrogyria
Disease Ontology
DOID:0080923
Mondo Disease Ontology
ORDO
OMIM
GARD
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
9896 FIG4 FIG4 phosphoinositide 5-phosphatase
Displaying 1 entry
Gene ID Gene Symbol Description Source
33658 FIG4 FIG4 phosphoinositide 5-phosphatase
Displaying 1 entry
Gene ID Gene Symbol Description Source
855392 FIG4 phosphatidylinositol-3,5-bisphosphate 5-phosphatase
The Human Phenotype Ontology
Displaying entries 21 - 30 of 35 in total
HPO ID HPO Term
HP:0100852 Abnormal fear-induced behavior
HP:0001263 Global developmental delay
HP:0000708 Atypical behavior
HP:0007024 Pseudobulbar paralysis
HP:0000256 Macrocephaly
HP:0002194 Delayed gross motor development
HP:0001249 Intellectual disability
HP:0002126 Polymicrogyria
HP:0003577 Congenital onset
HP:0003621 Juvenile onset
Displaying 1 entry
Gene ID Gene Symbol Description
9896 FIG4 FIG4 phosphoinositide 5-phosphatase

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024