Human Phenotype Ontology 
Grandparent Node:
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EEG with abnormally slow frequencies (HP:0011203)help
Parent Node:
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EEG with focal slow activity (HP:0010843)help
..Starting node
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EEG with occipital slowing (HP:0011210)help
Term ID: 11210
Name: EEG with occipital slowing
Synonym:
Definition: Slowing in occipital areas of the scalp EEG.
Comments:
Reference: HP:0011210
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0011210HP:0011210EEG with occipital slowing0GNB1 CL E G H27824396OMIM:616973Mental retardation, autosomal dominant 4212


Genes (1) :GNB1

Diseases (1) :OMIM:616973
 

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