developmental and epileptic encephalopathy 96

Summary
Synonym
  • DEE96
Definition
A developmental and epileptic encephalopathy characterized by onset of seizures in the first days or weeks of life that has_material_basis_in heterozygous mutation in the NSF gene on chromosome 17q21.
Super Class
autosomal dominant disease developmental and epileptic encephalopathy
Disease Ontology
DOID:0070377
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
18195 Nsf N-ethylmaleimide sensitive fusion protein
The Human Phenotype Ontology
Displaying entries 41 - 50 of 53 in total
HPO ID HPO Term
HP:0009381 Short finger
HP:0010174 Broad phalanx of the toes
HP:0010818 Generalized tonic seizure
HP:0010819 Atonic seizure
HP:0010850 EEG with spike-wave complexes
HP:0010851 EEG with burst suppression
HP:0011169 Generalized clonic seizure
HP:0011190 Uni- and bilateral multifocal epileptiform discharges
HP:0012448 Delayed myelination
HP:0012469 Infantile spasms
Displaying all 2 entries
Gene ID Gene Symbol Description
51227 PIGP phosphatidylinositol glycan anchor biosynthesis class P
9091 PIGQ phosphatidylinositol glycan anchor biosynthesis class Q

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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: December 9, 2024