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 11 - 20 of 31 in total
HPO ID HPO Term
HP:0000664 Synophrys
HP:0012745 Short palpebral fissure
HP:0001290 Generalized hypotonia
HP:0000319 Smooth philtrum
HP:0002521 Hypsarrhythmia
HP:0000007 Autosomal recessive inheritance
HP:0001357 Plagiocephaly
HP:0009748 Large earlobe
HP:0000581 Blepharophimosis
HP:0011471 Gastrostomy tube feeding in infancy
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