Human Phenotype Ontology 
Grandparent Node:
expandEEG with focal epileptiform discharges (HP:0011185)help
Parent Node:
expandEEG with focal sharp slow waves (HP:0011195)help
..Starting node
..expandEEG with frontal sharp slow waves (HP:0011290)help
Term ID: 11290
Name: EEG with frontal sharp slow waves
Synonym:
Definition: EEG with sharp slow waves in the frontal region. Sharp slow waves are focal sharp transient waves of a duration between 80 and 200 msec followed by a slow wave.
Comments:
Reference: HP:0011290
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandEEG with central sharp slow waves (HP:0011291) help
..expandEEG with occipital sharp slow waves (HP:0011287) help
..expandEEG with parietal sharp slow waves (HP:0011288) help
..expandEEG with temporal sharp slow waves (HP:0011289) 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:0011290HP:0011290EEG with frontal sharp slow waves0SPATA5 CL E G H16637818119ORPHA:457351Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndromeHP:0040283 - Occasional19


Genes (1) :SPATA5

Diseases (1) :ORPHA:457351
 

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