ODCs

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3 OMIM references -
4 associated genes
No signs/symptoms info

COMMON GENES: 1
PROTEIN INTERACTIONS: 2

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

Familial short QT syndrome

Jervell and Lange-Nielsen syndrome


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	KCNQ1 KCNH2	(0.9) (0.73)	KCNE1 KCNE1

Citations in the biomedical literature:

Familial short QT syndrome		Jervell and Lange-Nielsen syndrome
	Synonym(s): - SQTS		Synonym(s): - Long QT interval - deafness

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

	Classification (ICD10): (no data available)		Classification (ICD10): - Diseases of the circulatory system -

	Epidemiological data: Class of prevalence: unknown Average age onset: variable 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: 3 OMIM references - No MeSH references		External references: 2 OMIM references - 1 MeSH reference: D029593

No signs/symptoms info available.