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 with generalized epileptiform discharges (HP:0011198)

Parent Node:
EEG with spike-wave complexes (HP:0010850)

..Starting node
..EEG with spike-wave complexes (<2.5 Hz) (HP:0010847)

Term ID:

10847

Name:

EEG with spike-wave complexes (<2.5 Hz)

Synonym:

Electroencephalogram demonstrated spike-slow wave discharges

Definition:

The presence of complexes of slow spikes and slow waves (<2.5 Hz) in electroencephalography (EEG).

Comments:

Reference:

HP:0010847

Genes and Diseases:

Child Nodes:

Sister Nodes:

EEG with irregular generalized spike and wave complexes (HP:0001326)

EEG with polyspike wave complexes (HP:0002392)

EEG with spike-wave complexes (2.5-3.5 Hz) (HP:0010848)

EEG with spike-wave complexes (>3.5 Hz) (HP:0010849)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0010847	HP:0010847	EEG with spike-wave complexes (<2.5 Hz)	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.