developmental and epileptic encephalopathy 84

Summary
Synonym
  • DEE84
  • Jamuar syndrome
  • early infantile epileptic encephalopathy 84
Definition
A developmental and epileptic encephalopathy characterized by onset in the first months or years of life of refractory seizures, severely impaired global development, impaired intellectual development, absent speech, and inability to walk that has_material_basis_in homozygous or compound heterozygous mutation in the UGDH gene on chromosome 4p14.
Super Class
autosomal recessive disease developmental and epileptic encephalopathy
External Links
Disease Ontology
DOID:0112219
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
7358 UGDH UDP-glucose 6-dehydrogenase
Displaying 1 entry
Gene ID Gene Symbol Description Source
38760 sgl sugarless
The Human Phenotype Ontology
Displaying entries 21 - 30 of 31 in total
HPO ID HPO Term
HP:0001284 Areflexia
HP:0000307 Pointed chin
HP:0002188 Delayed CNS myelination
HP:0200134 Epileptic encephalopathy
HP:0001332 Dystonia
HP:0000490 Deeply set eye
HP:0003487 Babinski sign
HP:0000252 Microcephaly
HP:0002119 Ventriculomegaly
HP:0011097 Epileptic spasm
Displaying 1 entry
Gene ID Gene Symbol Description
7358 UGDH UDP-glucose 6-dehydrogenase

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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