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 with constitutional variants (HP:0011176)

Grandparent Node:
EEG with diffuse acceleration (HP:0011202)

Parent Node:
Beta-EEG (HP:0011179)

..Starting node
..Partial beta-EEG (HP:0011180)

Term ID:

11180

Name:

Partial beta-EEG

Synonym:

Definition:

EEG dominated by diffuse beta waves (>13 Hz) with occipitally localized alpha waves (8-13 Hz).

Comments:

Reference:

HP:0011180

Genes and Diseases:

Child Nodes:

Sister Nodes:

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0011180	HP:0011180	Partial beta-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.