ODCs

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1 OMIM reference -
2 associated genes
No signs/symptoms info

COMMON GENES: 1
PROTEIN INTERACTIONS: 1

4 OMIM references -
2 associated genes
5 signs/symptoms

Benign familial neonatal-infantile seizures

Benign familial neonatal seizures

KCNQ2	(UniProt - OMIM)		KCNQ2	(UniProt - OMIM)
SCN2A	(UniProt - OMIM)		KCNQ3	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	KCNQ2	(0.83)	KCNQ3

Citations in the biomedical literature:

Benign familial neonatal-infantile seizures		Benign familial neonatal seizures
	Synonym(s): - BFNIS - Benign neonatal-infantile epilepsy		Synonym(s): - Benign familial neonatal convulsions - Benign familial neonatal epilepsy

	Classification (Orphanet): - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare genetic disease - Rare neurologic disease

	Classification (ICD10): - Diseases of the nervous system -		Classification (ICD10): - Diseases of the nervous system -

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: normal Type of inheritance: autosomal dominant

	External references: 1 OMIM reference - No MeSH references		External references: 4 OMIM references - 2 MeSH references: C535466 / D020936

Benign familial neonatal seizures
	Very frequent - Autosomal dominant inheritance - Autosomal recessive inheritance - Hypertonia / spasticity / rigidity / stiffness - Seizures / epilepsy / absences / spasms / status epilepticus Occasional - Intellectual deficit / mental / psychomotor retardation / learning disability
Benign familial neonatal-infantile seizures
(no data available)