Human Phenotype Ontology

Hello! Guest! Please Login or Register! Clinician Mode

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
..Alpha-EEG (HP:0011178)

Term ID:

11178

Name:

Alpha-EEG

Synonym:

Definition:

EEG dominated by diffuse alpha-waves (8-13Hz).

Comments:

Reference:

HP:0011178

Genes and Diseases:

Child Nodes:

Sister Nodes:

Beta-EEG (HP:0011179)

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

EEG with persistent abnormal rhythmic activity (HP:0010846)

Low voltage EEG (HP:0011181)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0011178	HP:0011178	Alpha-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.