EEGL
MCID: ELC002
MIFTS: 15

Electroencephalogram, Low-Voltage (EEGL)

Aliases & Classifications for Electroencephalogram, Low-Voltage

MalaCards integrated aliases for Electroencephalogram, Low-Voltage:

Name: Electroencephalogram, Low-Voltage 57
Electroencephalographic Variant Pattern 1; Eegv1 57
Electro-Encephalographic Variant Pattern-1 13
Electroencephalographic Variant Pattern 1 57
Eeg, Low-Voltage; Eegl 57
Eeg, Low-Voltage 57
Eegv1 57
Eegl 57

Characteristics:

OMIM®:

57 (Updated 05-Mar-2021)
Inheritance:
autosomal dominant (20q)


HPO:

31
electroencephalogram, low-voltage:
Inheritance autosomal dominant inheritance


External Ids:

OMIM® 57 130180
MedGen 41 C1851759
SNOMED-CT via HPO 68 263681008

Summaries for Electroencephalogram, Low-Voltage

OMIM® : 57 This EEG variant is characterized by almost complete absence of alpha waves except, in some cases, for a few seconds after the eyes are closed and after hyperventilation (summary by Vogel and Motulsky, 1986). (130180) (Updated 05-Mar-2021)

MalaCards based summary : Electroencephalogram, Low-Voltage, also known as electroencephalographic variant pattern 1; eegv1, is related to alcohol dependence and anxiety. An important gene associated with Electroencephalogram, Low-Voltage is EEGV1 (Electro-Encephalographic Variant Pattern 1). Related phenotype is low voltage eeg.

Related Diseases for Electroencephalogram, Low-Voltage

Diseases related to Electroencephalogram, Low-Voltage via text searches within MalaCards or GeneCards Suite gene sharing:

# Related Disease Score Top Affiliating Genes
1 alcohol dependence 10.0
2 anxiety 10.0
3 immunoglobulin e concentration, serum 9.9
4 epilepsy, myoclonic juvenile 9.9
5 epilepsy, juvenile absence 1 9.9
6 epilepsy, idiopathic generalized 10 9.9
7 juvenile absence epilepsy 9.9
8 childhood absence epilepsy 9.9
9 early myoclonic encephalopathy 9.9

Graphical network of the top 20 diseases related to Electroencephalogram, Low-Voltage:



Diseases related to Electroencephalogram, Low-Voltage

Symptoms & Phenotypes for Electroencephalogram, Low-Voltage

Human phenotypes related to Electroencephalogram, Low-Voltage:

31
# Description HPO Frequency HPO Source Accession
1 low voltage eeg 31 HP:0011181

Symptoms via clinical synopsis from OMIM®:

57 (Updated 05-Mar-2021)
Lab:
low-voltage eeg
absent eeg alpha waves

Clinical features from OMIM®:

130180 (Updated 05-Mar-2021)

Drugs & Therapeutics for Electroencephalogram, Low-Voltage

Interventional clinical trials:


# Name Status NCT ID Phase Drugs
1 Self Abrading Rapidly Applied (SARA) Electrode Phase II Completed NCT02200523

Search NIH Clinical Center for Electroencephalogram, Low-Voltage

Genetic Tests for Electroencephalogram, Low-Voltage

Anatomical Context for Electroencephalogram, Low-Voltage

Publications for Electroencephalogram, Low-Voltage

Articles related to Electroencephalogram, Low-Voltage:

# Title Authors PMID Year
1
D20S19, linked to low voltage EEG, benign neonatal convulsions, and Fanconi anaemia, maps to a region of enhanced recombination and is localized between CpG islands. 57
1303209 1992
2
Confirmation of linkage of benign familial neonatal convulsions to D20S19 and D20S20. 57
1577466 1992
3
Localization of a gene for the human low-voltage EEG on 20q and genetic heterogeneity. 57
1346390 1992
4
Benign familial neonatal convulsions: evidence for clinical and genetic heterogeneity. 57
1859177 1991
5
The incidence of some inherited EEG variants in normal Japanese and German males. 57
5770378 1969
6
Common subtypes of idiopathic generalized epilepsies: lack of linkage to D20S19 close to candidate loci (EBN1, EEGV1) on chromosome 20. 61
8678111 1996
7
A genetic study of the human low-voltage electroencephalogram. 61
1427795 1992

Variations for Electroencephalogram, Low-Voltage

Expression for Electroencephalogram, Low-Voltage

Search GEO for disease gene expression data for Electroencephalogram, Low-Voltage.

Pathways for Electroencephalogram, Low-Voltage

GO Terms for Electroencephalogram, Low-Voltage

Sources for Electroencephalogram, Low-Voltage

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 EFO
18 ExPASy
19 FMA
20 GARD
28 GO
29 GTR
30 HMDB
31 HPO
32 ICD10
33 ICD10 via Orphanet
34 ICD9CM
35 IUPHAR
36 KEGG
37 LifeMap
39 LOVD
41 MedGen
44 MeSH
45 MESH via Orphanet
46 MGI
49 NCI
50 NCIt
51 NDF-RT
53 NINDS
54 Novoseek
56 OMIM via Orphanet
57 OMIM® (Updated 05-Mar-2021)
61 PubMed
63 QIAGEN
68 SNOMED-CT via HPO
69 TGDB
70 Tocris
71 UMLS
72 UMLS via Orphanet
Content
Loading form....