ODCs

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

PROTEIN INTERACTIONS: 1

2 OMIM references -
2 associated genes
No signs/symptoms info

Benign familial neonatal-infantile seizures

Jervell and Lange-Nielsen syndrome

KCNQ2	(UniProt - OMIM)		KCNE1	(UniProt - OMIM)
SCN2A	(UniProt - OMIM)		KCNQ1	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	KCNQ2	(0.72)	KCNQ1

Citations in the biomedical literature:

Benign familial neonatal-infantile seizures		Jervell and Lange-Nielsen syndrome
	Synonym(s): - BFNIS - Benign neonatal-infantile epilepsy		Synonym(s): - Long QT interval - deafness

	Classification (Orphanet): - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare cardiac disease - Rare developmental defect during embryogenesis - Rare genetic disease - Rare otorhinolaryngologic disease

	Classification (ICD10): - Diseases of the nervous system -		Classification (ICD10): - Diseases of the circulatory 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: 1-9 / 1 000 000 Average age onset: childhood Average age of death: - Type of inheritance: autosomal recessive

	External references: 1 OMIM reference - No MeSH references		External references: 2 OMIM references - 1 MeSH reference: D029593

No signs/symptoms info available.