developmental and epileptic encephalopathy 103

Summary
Synonym
  • DEE103
  • early infantile epileptic encephalopathy 103
Definition
A developmental and epileptic encephalopathy characterized by onset of various types of seizures in the first year of life that has_material_basis_in heterozygous mutation in the KCNC2 gene on chromosome 12q21.
Super Class
autosomal dominant disease developmental and epileptic encephalopathy
Disease Ontology
DOID:0070389
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
3747 KCNC2 potassium voltage-gated channel subfamily C member 2
Displaying 1 entry
Gene ID Gene Symbol Description Source
268345 Kcnc2 potassium voltage gated channel, Shaw-related subfamily, member 2
Displaying 1 entry
Gene ID Gene Symbol Description Source
246153 Kcnc2 potassium voltage-gated channel subfamily C member 2
Displaying 1 entry
Gene ID Gene Symbol Description Source
33599 Shaw Shaker cognate w
The Human Phenotype Ontology
Displaying entries 11 - 20 of 48 in total
HPO ID HPO Term
HP:0000508 Ptosis
HP:0001251 Ataxia
HP:0000639 Nystagmus
HP:0000494 Downslanted palpebral fissures
HP:0000717 Autism
HP:0001315 Reduced tendon reflexes
HP:0002133 Status epilepticus
HP:0001268 Mental deterioration
HP:0001558 Decreased fetal movement
HP:0001263 Global developmental delay
Displaying all 5 entries
Gene ID Gene Symbol Description
1759 DNM1 dynamin 1
523 ATP6V1A ATPase H+ transporting V1 subunit A
781 CACNA2D1 calcium voltage-gated channel auxiliary subunit alpha2delta 1
79947 DHDDS dehydrodolichyl diphosphate synthase subunit
8867 SYNJ1 synaptojanin 1

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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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