developmental and epileptic encephalopathy 107

Summary
Synonym
  • DEE107
  • early infantile epileptic encephalopathy 107
Definition
A developmental and epileptic encephalopathy characterized by onset of seizures in the first months of life, severe global developmental delay, profound intellectual disability, progressive microcephaly, and hypotonia that has_material_basis_in homozygous mutation in the NAPB gene on chromosome 20p11.
Super Class
autosomal recessive disease developmental and epileptic encephalopathy
Disease Ontology
DOID:0070393
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
17957 Napb N-ethylmaleimide sensitive fusion protein attachment protein beta
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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