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 31 - 40 of 48 in total
HPO ID HPO Term
HP:0001298 Encephalopathy
HP:0002063 Rigidity
HP:0001265 Hyporeflexia
HP:0001508 Failure to thrive
HP:0011443 Abnormality of coordination
HP:0004305 Involuntary movements
HP:0012547 Abnormal involuntary eye movements
HP:0002509 Limb hypertonia
HP:0012444 Brain atrophy
HP:0100710 Impulsivity
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

About Release Notes Help Feedback

International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.1.0

Last updated: December 9, 2024