bilateral frontoparietal polymicrogyria

Summary
Definition
A polymicrogyria that is characterized by excessive cortical folding and abnormal cortical layering, that involves the frontoparietal region of the brain and that presents with hypotonia, developmental delay, moderate to severe intellectual disability, pyramidal signs, epileptic seizures, non progressive cerebellar ataxia, dysconjugate gaze and/or strabismus and that has_material_basis_in homozygous mutation in the ADGRG1 gene on chromosome 16q21.
Super Class
autosomal recessive disease polymicrogyria
Disease Ontology
DOID:0080922
Mondo Disease Ontology
NCI Thesaurus
OMIM
GARD
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
9289 ADGRG1 adhesion G protein-coupled receptor G1
Displaying 1 entry
Gene ID Gene Symbol Description Source
14766 Adgrg1 adhesion G protein-coupled receptor G1
The Human Phenotype Ontology
Displaying entries 21 - 22 of 22 in total
HPO ID HPO Term
HP:0001250 Seizure
HP:0002365 Hypoplasia of the brainstem
Displaying 1 entry
Gene ID Gene Symbol Description
5728 PTEN phosphatase and tensin homolog

About Release Notes Help Feedback

Click here to visit the beta site.


International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

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


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.1.0

Last updated: December 9, 2024