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 abnormally slow frequencies (HP:0011203)

Parent Node:
EEG with generalized slow activity (HP:0010845)

..Starting node
..EEG with intermittent slow activity (HP:0011205)

Term ID:

11205

Name:

EEG with intermittent slow activity

Synonym:

Definition:

Non-continuous diffuse slowing of electroencephalographic patterns.

Comments:

Reference:

HP:0011205

Genes and Diseases:

Child Nodes:

Sister Nodes:

EEG with continuous slow activity (HP:0011204)

EEG with generalized slow activity grade 1 (HP:0011206)

EEG with generalized slow activity grade 2 (HP:0011207)

EEG with generalized slow activity grade 3 (HP:0011208)

EEG with generalized slow activity grade 4 (HP:0011209)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0011205	HP:0011205	EEG with intermittent slow 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.