Human Phenotype Ontology 
Grandparent Node:
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EEG abnormality (HP:0002353)help
Parent Node:
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EEG with constitutional variants (HP:0011176)help
..Starting node
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EEG with persistent abnormal rhythmic activity (HP:0010846)help
Term ID: 10846
Name: EEG with persistent abnormal rhythmic activity
Synonym: EEG: persistent abnormal rhythmic activity
Definition:
Comments:
Reference: HP:0010846
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAlpha-EEG (HP:0011178) help
..expandBeta-EEG (HP:0011179) help
..expandEEG with 4-5/second background activity (HP:0011177) help
..expandLow voltage EEG (HP:0011181) 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:0010846HP:0010846EEG with persistent abnormal rhythmic activity0GALC CL E G H25814115ORPHA:206443Late-infantile/juvenile Krabbe diseaseHP:0040282 - Frequent160
HP:0010846HP:0010846EEG with persistent abnormal rhythmic activity0PRNP CL E G H56219449ORPHA:282166Inherited Creutzfeldt-Jakob diseaseHP:0040282 - Frequent69


Genes (2) :GALC PRNP

Diseases (2) :ORPHA:206443 ORPHA:282166
 

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