Human Phenotype Ontology 
Grandparent Node:
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EEG with focal epileptiform discharges (HP:0011185)help
Parent Node:
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Multifocal epileptiform discharges (HP:0010841)help
..Starting node
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Uni- and bilateral multifocal epileptiform discharges (HP:0011190)help
Term ID: 11190
Name: Uni- and bilateral multifocal epileptiform discharges
Synonym:
Definition: Epileptiform discharges identified at multiple locations temporarily in both hemispheres and temporarily in one hemisphere.
Comments:
Reference: HP:0011190
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandBilateral multifocal epileptiform discharges (HP:0011189) help
..expandUnilateral multifocal epileptiform discharges (HP:0011191) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0011190HP:0011190Uni- and bilateral multifocal epileptiform discharges0ARX CL E G H17030218060ORPHA:1934Early infantile epileptic encephalopathyHP:0040283 - Occasional166
HP:0011190HP:0011190Uni- and bilateral multifocal epileptiform discharges0CASK CL E G H85731497ORPHA:1934Early infantile epileptic encephalopathyHP:0040283 - Occasional118
HP:0011190HP:0011190Uni- and bilateral multifocal epileptiform discharges0CDKL5 CL E G H679211411ORPHA:1934Early infantile epileptic encephalopathyHP:0040283 - Occasional405
HP:0011190HP:0011190Uni- and bilateral multifocal epileptiform discharges0DMXL2 CL E G H233122938ORPHA:1934Early infantile epileptic encephalopathyHP:0040283 - Occasional3
HP:0011190HP:0011190Uni- and bilateral multifocal epileptiform discharges0GNAO1 CL E G H27754389ORPHA:1934Early infantile epileptic encephalopathyHP:0040283 - Occasional36
HP:0011190HP:0011190Uni- and bilateral multifocal epileptiform discharges0GRIN1 CL E G H29024584ORPHA:1934Early infantile epileptic encephalopathyHP:0040283 - Occasional108
HP:0011190HP:0011190Uni- and bilateral multifocal epileptiform discharges0GRM7 CL E G H29174599ORPHA:1934Early infantile epileptic encephalopathyHP:0040283 - Occasional5
HP:0011190HP:0011190Uni- and bilateral multifocal epileptiform discharges0KCNA1 CL E G H37366218ORPHA:1934Early infantile epileptic encephalopathyHP:0040283 - Occasional145
HP:0011190HP:0011190Uni- and bilateral multifocal epileptiform discharges0NEUROD2 CL E G H47617763ORPHA:1934Early infantile epileptic encephalopathyHP:0040283 - Occasional
HP:0011190HP:0011190Uni- and bilateral multifocal epileptiform discharges0PIGP CL E G H512273046ORPHA:1934Early infantile epileptic encephalopathyHP:0040283 - Occasional2
HP:0011190HP:0011190Uni- and bilateral multifocal epileptiform discharges0PIGQ CL E G H909114135ORPHA:1934Early infantile epileptic encephalopathyHP:0040283 - Occasional3
HP:0011190HP:0011190Uni- and bilateral multifocal epileptiform discharges0PNKP CL E G H112849154ORPHA:1934Early infantile epileptic encephalopathyHP:0040283 - Occasional244
HP:0011190HP:0011190Uni- and bilateral multifocal epileptiform discharges0SCN1B CL E G H632410586ORPHA:1934Early infantile epileptic encephalopathyHP:0040283 - Occasional126
HP:0011190HP:0011190Uni- and bilateral multifocal epileptiform discharges0SCN2A CL E G H632610588ORPHA:1934Early infantile epileptic encephalopathyHP:0040283 - Occasional427
HP:0011190HP:0011190Uni- and bilateral multifocal epileptiform discharges0SIK1 CL E G H15009411142ORPHA:1934Early infantile epileptic encephalopathyHP:0040283 - Occasional11
HP:0011190HP:0011190Uni- and bilateral multifocal epileptiform discharges0SLC25A22 CL E G H7975119954ORPHA:1934Early infantile epileptic encephalopathyHP:0040283 - Occasional166
HP:0011190HP:0011190Uni- and bilateral multifocal epileptiform discharges0TRIM8 CL E G H8160315579ORPHA:1934Early infantile epileptic encephalopathyHP:0040283 - Occasional1


Genes (17) :ARX CASK CDKL5 DMXL2 GNAO1 GRIN1 GRM7 KCNA1 NEUROD2 PIGP PIGQ PNKP SCN1B SCN2A SIK1 SLC25A22 TRIM8

Diseases (1) :ORPHA:1934
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.