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
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 1 - 10 of 31 in total
HPO ID HPO Term
HP:0002033 Poor suck
HP:0000639 Nystagmus
HP:0002857 Genu valgum
HP:0000340 Sloping forehead
HP:0002205 Recurrent respiratory infections
HP:0008936 Axial hypotonia
HP:0001257 Spasticity
HP:0000252 Microcephaly
HP:0002120 Cerebral cortical atrophy
HP:0007750 Hypoplasia of the fovea
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: December 9, 2024