developmental and epileptic encephalopathy 83

Summary
Synonym
  • DEE83
  • early infantile epileptic encephalopathy 83
Definition
A developmental and epileptic encephalopathy characterized by onset in the first days or months of life of frequent, usually refractory, seizures and profoundly impaired development that has_material_basis_in homozygous or compound heterozygous mutation in the UGP2 gene on chromosome 2p15.
Super Class
autosomal recessive disease developmental and epileptic encephalopathy
External Links
Disease Ontology
DOID:0112218
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
7360 UGP2 UDP-glucose pyrophosphorylase 2
Displaying 1 entry
Gene ID Gene Symbol Description Source
216558 Ugp2 UDP-glucose pyrophosphorylase 2
Displaying 1 entry
Gene ID Gene Symbol Description Source
853830 UGP1 UTP glucose-1-phosphate uridylyltransferase
The Human Phenotype Ontology
Displaying entries 21 - 30 of 31 in total
HPO ID HPO Term
HP:0001344 Absent speech
HP:0000341 Narrow forehead
HP:0002273 Tetraparesis
HP:0012450 Chronic constipation
HP:0002007 Frontal bossing
HP:0000369 Low-set ears
HP:0002553 Highly arched eyebrow
HP:0000286 Epicanthus
HP:0002187 Intellectual disability, profound
HP:0008872 Feeding difficulties in infancy
Displaying 1 entry
Gene ID Gene Symbol Description
7360 UGP2 UDP-glucose pyrophosphorylase 2

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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: August 19, 2024