Human Phenotype Ontology 
Grandparent Node:
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EEG with abnormally slow frequencies (HP:0011203)help
Parent Node:
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EEG with generalized slow activity (HP:0010845)help
..Starting node
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EEG with continuous slow activity (HP:0011204)help
Term ID: 11204
Name: EEG with continuous slow activity
Synonym:
Definition: EEG showing diffuse slowing without interruption.
Comments:
Reference: HP:0011204
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandEEG with generalized slow activity grade 1 (HP:0011206) help
..expandEEG with generalized slow activity grade 2 (HP:0011207) help
..expandEEG with generalized slow activity grade 3 (HP:0011208) help
..expandEEG with generalized slow activity grade 4 (HP:0011209) help
..expandEEG with intermittent slow activity (HP:0011205) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0011204HP:0011204EEG with continuous slow activity0C9ORF72 CL E G H20322828337ORPHA:275864Behavioral variant of frontotemporal dementiaHP:0040282 - Frequent56
HP:0011204HP:0011204EEG with continuous slow activity0C9ORF72 CL E G H20322828337ORPHA:100070Progressive non-fluent aphasiaHP:0040282 - Frequent56
HP:0011204HP:0011204EEG with continuous slow activity0CHMP2B CL E G H2597824537ORPHA:275864Behavioral variant of frontotemporal dementiaHP:0040282 - Frequent42
HP:0011204HP:0011204EEG with continuous slow activity0CHMP2B CL E G H2597824537ORPHA:100070Progressive non-fluent aphasiaHP:0040282 - Frequent42
HP:0011204HP:0011204EEG with continuous slow activity0GRN CL E G H28964601ORPHA:275864Behavioral variant of frontotemporal dementiaHP:0040282 - Frequent126
HP:0011204HP:0011204EEG with continuous slow activity0GRN CL E G H28964601ORPHA:100070Progressive non-fluent aphasiaHP:0040282 - Frequent126
HP:0011204HP:0011204EEG with continuous slow activity0MAPT CL E G H41376893ORPHA:275864Behavioral variant of frontotemporal dementiaHP:0040282 - Frequent140
HP:0011204HP:0011204EEG with continuous slow activity0MAPT CL E G H41376893ORPHA:100070Progressive non-fluent aphasiaHP:0040282 - Frequent140
HP:0011204HP:0011204EEG with continuous slow activity0PSEN1 CL E G H56639508ORPHA:275864Behavioral variant of frontotemporal dementiaHP:0040282 - Frequent241
HP:0011204HP:0011204EEG with continuous slow activity0PSEN1 CL E G H56639508ORPHA:100070Progressive non-fluent aphasiaHP:0040282 - Frequent241
HP:0011204HP:0011204EEG with continuous slow activity0SQSTM1 CL E G H887811280ORPHA:275864Behavioral variant of frontotemporal dementiaHP:0040282 - Frequent62
HP:0011204HP:0011204EEG with continuous slow activity0TMEM106B CL E G H5466422407ORPHA:275864Behavioral variant of frontotemporal dementiaHP:0040282 - Frequent
HP:0011204HP:0011204EEG with continuous slow activity0TMEM106B CL E G H5466422407ORPHA:100070Progressive non-fluent aphasiaHP:0040282 - Frequent
HP:0011204HP:0011204EEG with continuous slow activity0TREM2 CL E G H5420917761ORPHA:275864Behavioral variant of frontotemporal dementiaHP:0040282 - Frequent31
HP:0011204HP:0011204EEG with continuous slow activity0TREM2 CL E G H5420917761ORPHA:100070Progressive non-fluent aphasiaHP:0040282 - Frequent31
HP:0011204HP:0011204EEG with continuous slow activity0VCP CL E G H741512666ORPHA:275864Behavioral variant of frontotemporal dementiaHP:0040282 - Frequent63
HP:0011204HP:0011204EEG with continuous slow activity0VCP CL E G H741512666ORPHA:100070Progressive non-fluent aphasiaHP:0040282 - Frequent63


Genes (9) :C9ORF72 CHMP2B GRN MAPT PSEN1 SQSTM1 TMEM106B TREM2 VCP

Diseases (2) :ORPHA:275864 ORPHA:100070
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.