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Diseases

Benign neonatal epilepsy

benign neonatal epilepsy

Entity Type
Diseases
Relation Groups
1
Relation Preview
8

Basic Information

Grouped by core information, identifiers, and descriptions.

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Core Information

Disease Name
Benign neonatal epilepsy
Standard Disease Name
benign neonatal epilepsy
MeSH Tree
No data
ICD-10
No data

Identifiers

DO ID
No data
MeSH ID
D020936
OMIM ID
No data
UMLS ID
C0270851
HPO ID
No data

Description and Extensions

Description
NCI2016_02D:An inherited or sporadic disorder characterized by epileptic seizures in the first four to six weeks of life. The seizures tend to subside after the fifteenth week of life.|MSH2017_2016_08_12:A condition marked by recurrent seizures that occur during the first 4-6 weeks of life despite an otherwise benign neonatal course. Autosomal dominant familial and sporadic forms have been identified. Seizures generally consist of brief episodes of tonic posturing and other movements, apnea, eye deviations, and blood pressure fluctuations. These tend to remit after the 6th week of life. The risk of developing epilepsy at an older age is moderately increased in the familial form of this disorder. (Neurologia 1996 Feb;11(2):51-5)
Related

Direct relations and traceable candidates grouped by relation type.

Related Targets

target disease8 Targets
01
KCNA1
potassium voltage-gated channel subfamily A member 1
potassium voltage-gated channel subfamily A member 1
02
KCNA2
potassium voltage-gated channel subfamily A member 2
potassium voltage-gated channel subfamily A member 2
03
KCNQ2
potassium voltage-gated channel subfamily Q member 2
potassium voltage-gated channel subfamily Q member 2
04
KCNQ3
potassium voltage-gated channel subfamily Q member 3
potassium voltage-gated channel subfamily Q member 3