Human Phenotype Ontology

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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Grandparent Node:
EEG abnormality (HP:0002353)

Parent Node:
EEG with constitutional variants (HP:0011176)

..Starting node
..Low voltage EEG (HP:0011181)

Term ID:

11181

Name:

Low voltage EEG

Synonym:

Definition:

EEG with an amplitude less than 30 microvolts without observable occipital alpha rhythm (8-13 Hz).

Comments:

Reference:

HP:0011181

Genes and Diseases:

Child Nodes:

Sister Nodes:

Alpha-EEG (HP:0011178)

Beta-EEG (HP:0011179)

EEG with 4-5/second background activity (HP:0011177)

EEG with persistent abnormal rhythmic activity (HP:0010846)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0011181	HP:0011181	Low voltage EEG	0	CL E G H

Genes (0) :

Diseases (0) :

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