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 changes in voltage (HP:0011201)

..Starting node
..EEG with localized low amplitude activity (HP:0010855)

Term ID:

10855

Name:

EEG with localized low amplitude activity

Synonym:

EEG with localised low amplitude activity; EEG: localised low amplitude activity

Definition:

An abnormal localized reduction in amplitude of the cerebral electrical activity recorded along the scalp by electroencephalography (EEG).

Comments:

Reference:

HP:0010855

Genes and Diseases:

Child Nodes:

Sister Nodes:

EEG with generalized low amplitude activity (HP:0010854)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0010855	HP:0010855	EEG with localized low amplitude activity	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.